nsv817612

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,293,908

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 16417 SVs from 71 studies. See in: genome view    
Remapped(Score: Good):31,996,213-46,290,120Question Mark
Overlapping variant regions from other studies: 16426 SVs from 71 studies. See in: genome view    
Remapped(Score: Good):30,584,016-44,918,759Question Mark
Overlapping variant regions from other studies: 8715 SVs from 36 studies. See in: genome view    
Submitted genomic30,047,677-44,352,166Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv817612RemappedGoodGRCh38 (hg38)Primary AssemblyFirst PassNC_000020.11Chr2031,996,21331,996,21346,290,12046,290,120
nsv817612RemappedGoodGRCh37 (hg19)Primary AssemblyFirst PassNC_000020.10Chr2030,584,01630,584,01644,918,75944,918,759
nsv817612Submitted genomicNCBI36 (hg18)NC_000020.9Chr2030,047,67730,506,00944,328,69344,352,166

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysis
nssv1415556copy number loss340SNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1415556RemappedGoodNC_000020.11:g.(31
996213_31996213)_(
46290120_46290120)
del
GRCh38 (hg38)Primary AssemblyFirst PassNC_000020.11Chr2031,996,21331,996,21346,290,12046,290,120
nssv1415556RemappedGoodNC_000020.10:g.(30
584016_30584016)_(
44918759_44918759)
del
GRCh37 (hg19)Primary AssemblyFirst PassNC_000020.10Chr2030,584,01630,584,01644,918,75944,918,759
nssv1415556Submitted genomicNC_000020.9:g.(300
47677_30506009)_(4
4328693_44352166)d
el
NCBI36 (hg18)NC_000020.9Chr2030,047,67730,506,00944,328,69344,352,166

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant