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nsv6450577

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:649,879

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2495 SVs from 114 studies. See in: genome view    
    Submitted genomic4,619,075-5,268,953Question Mark
    Overlapping variant regions from other studies: 2495 SVs from 114 studies. See in: genome view    
    Remapped(Score: Perfect):4,640,305-5,290,183Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6450577Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr114,619,0755,268,953
    nsv6450577RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr114,640,3055,290,183

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18182276duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18182276Submitted genomicNC_000011.10:g.461
    9075_5268953dup
    GRCh38 (hg38)NC_000011.10Chr114,619,0755,268,953
    nssv18182276RemappedPerfectNC_000011.9:g.4640
    305_5290183dup
    GRCh37.p13First PassNC_000011.9Chr114,640,3055,290,183

    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)
    nssv18182276<0.001139256
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