nsv821613

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,561

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 328 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):130,048,819-130,050,379Question Mark
Overlapping variant regions from other studies: 328 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):131,061,065-131,062,625Question Mark
Overlapping variant regions from other studies: 222 SVs from 15 studies. See in: genome view    
Submitted genomic131,130,247-131,131,807Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv821613RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000008.11Chr8130,048,819130,050,379
nsv821613RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000008.10Chr8131,061,065131,062,625
nsv821613Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000008.9Chr8131,130,247131,131,807

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1420779deletionNA10851SequencingRead depth1,299

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1420779RemappedPerfectNC_000008.11:g.(?_
130048819)_(130050
379_?)del
GRCh38 (hg38)First PassNC_000008.11Chr8130,048,819130,050,379
nssv1420779RemappedPerfectNC_000008.10:g.(?_
131061065)_(131062
625_?)del
GRCh37 (hg19)First PassNC_000008.10Chr8131,061,065131,062,625
nssv1420779Submitted genomicNC_000008.9:g.(?_1
31130247)_(1311318
07_?)del
NCBI36 (hg18)NC_000008.9Chr8131,130,247131,131,807

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

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