U.S. flag

An official website of the United States government

nsv6778440

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:196,582

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 534 SVs from 45 studies. See in: genome view    
    Submitted genomic139,104,141-139,300,722Question Mark
    Overlapping variant regions from other studies: 534 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):138,439,830-138,636,411Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6778440Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5139,104,141139,300,722
    nsv6778440RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5138,439,830138,636,411

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18694826duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18694826Submitted genomicNC_000005.10:g.139
    104141_139300722du
    p
    GRCh38 (hg38)NC_000005.10Chr5139,104,141139,300,722
    nssv18694826RemappedPerfectNC_000005.9:g.1384
    39830_138636411dup
    GRCh37.p13First PassNC_000005.9Chr5138,439,830138,636,411

    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)
    nssv186948264e-061275722
    Support Center