U.S. flag

An official website of the United States government

nsv6171560

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:182

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 29 studies. See in: genome view    
Submitted genomic129,340,574-129,340,755Question Mark
Overlapping variant regions from other studies: 136 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):132,102,853-132,103,034Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6171560Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9129,340,574129,340,755
nsv6171560RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9132,102,853132,103,034

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17905742deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17905742Submitted genomicNC_000009.12:g.129
340574_129340755de
l
GRCh38 (hg38)NC_000009.12Chr9129,340,574129,340,755
nssv17905742RemappedPerfectNC_000009.11:g.132
102853_132103034de
l
GRCh37.p13First PassNC_000009.11Chr9132,102,853132,103,034

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)
nssv179057420.004102268
Support Center