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nsv6776604

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:273,285

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 578 SVs from 53 studies. See in: genome view    
    Submitted genomic38,259,807-38,533,091Question Mark
    Overlapping variant regions from other studies: 578 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):38,259,909-38,533,193Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6776604Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr538,259,80738,533,091
    nsv6776604RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr538,259,90938,533,193

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18704152duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18704152Submitted genomicNC_000005.10:g.382
    59807_38533091dup
    GRCh38 (hg38)NC_000005.10Chr538,259,80738,533,091
    nssv18704152RemappedPerfectNC_000005.9:g.3825
    9909_38533193dup
    GRCh37.p13First PassNC_000005.9Chr538,259,90938,533,193

    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)
    nssv187041524e-061275808
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