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nsv5629187

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 128 SVs from 33 studies. See in: genome view    
Submitted genomic23,729,555-23,729,555Question Mark
Overlapping variant regions from other studies: 128 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):23,769,174-23,769,174Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5629187Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr723,729,55523,729,555
nsv5629187RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr723,769,17423,769,174

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17143261insertionHG03125SequencingSequence alignment5,031

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17143261Submitted genomicNC_000007.14:g.237
29555_23729556ins8
6
GRCh38 (hg38)NC_000007.14Chr723,729,55523,729,555
nssv17143261RemappedPerfectNC_000007.13:g.237
69174_23769175ins8
6
GRCh37.p13First PassNC_000007.13Chr723,769,17423,769,174

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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