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nsv7039987

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,352,905

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7997 SVs from 92 studies. See in: genome view    
    Submitted genomic145,076,609-150,429,513Question Mark
    Overlapping variant regions from other studies: 7954 SVs from 92 studies. See in: genome view    
    Remapped(Score: Good):144,158,129-149,597,776Question Mark
    Overlapping variant regions from other studies: 3588 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):601,002-5,953,911Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039987Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX145,076,609150,429,513
    nsv7039987RemappedGoodGRCh37.p13Primary AssemblySecond PassNC_000023.10ChrX144,158,129149,597,776
    nsv7039987RemappedPerfectGRCh37.p13PATCHESFirst PassNW_004070890.2ChrX|NW_00
    4070890.2
    601,0025,953,911

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18763433inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18763433Submitted genomicNC_000023.11:g.145
    076609_150429513in
    v
    GRCh38 (hg38)NC_000023.11ChrX145,076,609150,429,513
    nssv18763433RemappedPerfectNW_004070890.2:g.6
    01002_5953911inv
    GRCh37.p13First PassNW_004070890.2ChrX|NW_00
    4070890.2
    601,0025,953,911
    nssv18763433RemappedGoodNC_000023.10:g.144
    158129_149597776in
    v
    GRCh37.p13Second PassNC_000023.10ChrX144,158,129149,597,776

    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)
    nssv187634339e-062222222
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