U.S. flag

An official website of the United States government

nsv5528628

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,854

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 128 SVs from 32 studies. See in: genome view    
Submitted genomic69,029,752-69,032,605Question Mark
Overlapping variant regions from other studies: 128 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):69,063,655-69,066,508Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528628Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1669,029,75269,032,605
nsv5528628RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1669,063,65569,066,508

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17708527deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17708527Submitted genomicNC_000016.10:g.690
29752_69032605del
GRCh38 (hg38)NC_000016.10Chr1669,029,75269,032,605
nssv17708527RemappedPerfectNC_000016.9:g.6906
3655_69066508del
GRCh37.p13First PassNC_000016.9Chr1669,063,65569,066,508

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv177085270.012806404
Support Center