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nsv5525355

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,557

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 246 SVs from 33 studies. See in: genome view    
Submitted genomic76,550,542-76,584,098Question Mark
Overlapping variant regions from other studies: 246 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):74,546,624-74,580,180Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5525355Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1776,550,54276,584,098
nsv5525355RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1774,546,62474,580,180

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714734duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714734Submitted genomicNC_000017.11:g.765
50542_76584098dup
GRCh38 (hg38)NC_000017.11Chr1776,550,54276,584,098
nssv17714734RemappedPerfectNC_000017.10:g.745
46624_74580180dup
GRCh37.p13First PassNC_000017.10Chr1774,546,62474,580,180

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)
nssv17714734<0.00116404
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