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nsv6138921

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,894

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 454 SVs from 18 studies. See in: genome view    
Submitted genomic23,139,388-23,145,281Question Mark
Overlapping variant regions from other studies: 455 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):25,285,535-25,291,428Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6138921Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000024.10ChrY23,139,38823,145,281
nsv6138921RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000024.9ChrY25,285,53525,291,428

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17742977duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17742977Submitted genomicNC_000024.10:g.231
39388_23145281dup
GRCh38 (hg38)NC_000024.10ChrY23,139,38823,145,281
nssv17742977RemappedPerfectNC_000024.9:g.2528
5535_25291428dup
GRCh37.p13First PassNC_000024.9ChrY25,285,53525,291,428

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)
nssv177429770.0055929
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