U.S. flag

An official website of the United States government

nsv6790478

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,505,137

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6548 SVs from 97 studies. See in: genome view    
    Submitted genomic36,549,033-39,054,169Question Mark
    Overlapping variant regions from other studies: 6548 SVs from 97 studies. See in: genome view    
    Remapped(Score: Perfect):36,516,810-39,021,945Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6790478Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr636,549,03339,054,169
    nsv6790478RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr636,516,81039,021,945

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18714973duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18714973Submitted genomicNC_000006.12:g.365
    49033_39054169dup
    GRCh38 (hg38)NC_000006.12Chr636,549,03339,054,169
    nssv18714973RemappedPerfectNC_000006.11:g.365
    16810_39021945dup
    GRCh37.p13First PassNC_000006.11Chr636,516,81039,021,945

    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)
    nssv187149734e-061275824
    Support Center