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nsv6507008

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:48,968

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 203 SVs from 39 studies. See in: genome view    
    Submitted genomic93,993,836-94,042,803Question Mark
    Overlapping variant regions from other studies: 207 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):94,460,182-94,509,149Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6507008Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1493,993,83694,042,803
    nsv6507008RemappedPerfectGRCh37.p13Primary AssemblySecond PassNC_000014.8Chr1494,460,18294,509,149

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18194189duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18194189Submitted genomicNC_000014.9:g.9399
    3836_94042803dup
    GRCh38 (hg38)NC_000014.9Chr1493,993,83694,042,803
    nssv18194189RemappedPerfectNC_000014.8:g.9446
    0182_94509149dup
    GRCh37.p13Second PassNC_000014.8Chr1494,460,18294,509,149

    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)
    nssv18194189<0.001139294
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