nsv441696

  • Variant Calls:7
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,386

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 69 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):73,216,260-73,245,645Question Mark
Overlapping variant regions from other studies: 69 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):73,681,943-73,711,328Question Mark
Overlapping variant regions from other studies: 4 SVs from 3 studies. See in: genome view    
Submitted genomic73,393,964-73,423,349Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv441696RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr173,216,26073,245,645
nsv441696RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr173,681,94373,711,328
nsv441696Submitted genomicNCBI35 (hg17)NC_000001.8Chr173,393,96473,423,349

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls from this Sample
nssv1656671copy number gainNA19131SNP arrayProbe signal intensity3187
nssv1656672copy number gainNA19132SNP arrayProbe signal intensity3176
nssv1656673copy number gainNA19137SNP arrayProbe signal intensity3210
nssv1656674copy number gainNA19144SNP arrayProbe signal intensity3179
nssv1656675copy number gainNA19193SNP arrayProbe signal intensity3180
nssv1656676copy number gainNA19194SNP arrayProbe signal intensity3176
nssv1656677copy number gainNA19204SNP arrayProbe signal intensity3200

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nssv1656671RemappedPerfectNC_000001.11:g.(?_73216260)_(73245645_?)dupGRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr173,216,26073,245,645
nssv1656672RemappedPerfectNC_000001.11:g.(?_73216260)_(73245645_?)dupGRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr173,216,26073,245,645
nssv1656673RemappedPerfectNC_000001.11:g.(?_73216260)_(73245645_?)dupGRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr173,216,26073,245,645
nssv1656674RemappedPerfectNC_000001.11:g.(?_73216260)_(73245645_?)dupGRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr173,216,26073,245,645
nssv1656675RemappedPerfectNC_000001.11:g.(?_73216260)_(73245645_?)dupGRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr173,216,26073,245,645
nssv1656676RemappedPerfectNC_000001.11:g.(?_73216260)_(73245645_?)dupGRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr173,216,26073,245,645
nssv1656677RemappedPerfectNC_000001.11:g.(?_73216260)_(73245645_?)dupGRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr173,216,26073,245,645
nssv1656671RemappedPerfectNC_000001.10:g.(?_73681943)_(73711328_?)dupGRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr173,681,94373,711,328
nssv1656672RemappedPerfectNC_000001.10:g.(?_73681943)_(73711328_?)dupGRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr173,681,94373,711,328
nssv1656673RemappedPerfectNC_000001.10:g.(?_73681943)_(73711328_?)dupGRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr173,681,94373,711,328
nssv1656674RemappedPerfectNC_000001.10:g.(?_73681943)_(73711328_?)dupGRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr173,681,94373,711,328
nssv1656675RemappedPerfectNC_000001.10:g.(?_73681943)_(73711328_?)dupGRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr173,681,94373,711,328
nssv1656676RemappedPerfectNC_000001.10:g.(?_73681943)_(73711328_?)dupGRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr173,681,94373,711,328
nssv1656677RemappedPerfectNC_000001.10:g.(?_73681943)_(73711328_?)dupGRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr173,681,94373,711,328
nssv1656671Submitted genomicNC_000001.8:g.(?_73393964)_(73423349_?)dupNCBI35 (hg17)NC_000001.8Chr173,393,96473,423,349
nssv1656672Submitted genomicNC_000001.8:g.(?_73393964)_(73423349_?)dupNCBI35 (hg17)NC_000001.8Chr173,393,96473,423,349
nssv1656673Submitted genomicNC_000001.8:g.(?_73393964)_(73423349_?)dupNCBI35 (hg17)NC_000001.8Chr173,393,96473,423,349
nssv1656674Submitted genomicNC_000001.8:g.(?_73393964)_(73423349_?)dupNCBI35 (hg17)NC_000001.8Chr173,393,96473,423,349
nssv1656675Submitted genomicNC_000001.8:g.(?_73393964)_(73423349_?)dupNCBI35 (hg17)NC_000001.8Chr173,393,96473,423,349
nssv1656676Submitted genomicNC_000001.8:g.(?_73393964)_(73423349_?)dupNCBI35 (hg17)NC_000001.8Chr173,393,96473,423,349
nssv1656677Submitted genomicNC_000001.8:g.(?_73393964)_(73423349_?)dupNCBI35 (hg17)NC_000001.8Chr173,393,96473,423,349

There are no validations for this variant

There are no clinical assertions for this variant

There is no genotype information for this variant