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nsv5425602

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 317 SVs from 16 studies. See in: genome view    
Submitted genomic26,625,388-26,631,388Question Mark
Overlapping variant regions from other studies: 318 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):28,771,535-28,777,535Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5425602Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000024.10ChrY26,625,38826,631,388
nsv5425602RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000024.9ChrY28,771,53528,777,535

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17742999duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17742999Submitted genomicNC_000024.10:g.266
25388_26631388dup
GRCh38 (hg38)NC_000024.10ChrY26,625,38826,631,388
nssv17742999RemappedPerfectNC_000024.9:g.2877
1535_28777535dup
GRCh37.p13First PassNC_000024.9ChrY28,771,53528,777,535

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)
nssv177429990.00461577
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