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nsv5523938

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:125,817

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 556 SVs from 57 studies. See in: genome view    
Submitted genomic77,055,249-77,181,065Question Mark
Overlapping variant regions from other studies: 556 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):75,051,331-75,177,147Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523938Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1777,055,24977,181,065
nsv5523938RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1775,051,33175,177,147

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17725012duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17725012Submitted genomicNC_000017.11:g.770
55249_77181065dup
GRCh38 (hg38)NC_000017.11Chr1777,055,24977,181,065
nssv17725012RemappedPerfectNC_000017.10:g.750
51331_75177147dup
GRCh37.p13First PassNC_000017.10Chr1775,051,33175,177,147

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)
nssv17725012<0.00116404
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