U.S. flag

An official website of the United States government

nsv6919870

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:78,369

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 450 SVs from 61 studies. See in: genome view    
    Submitted genomic7,133,048-7,211,416Question Mark
    Overlapping variant regions from other studies: 450 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):7,285,644-7,364,012Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6919870Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr127,133,0487,211,416
    nsv6919870RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr127,285,6447,364,012

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18598851duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18598851Submitted genomicNC_000012.12:g.713
    3048_7211416dup
    GRCh38 (hg38)NC_000012.12Chr127,133,0487,211,416
    nssv18598851RemappedPerfectNC_000012.11:g.728
    5644_7364012dup
    GRCh37.p13First PassNC_000012.11Chr127,285,6447,364,012

    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)
    nssv185988514e-061274270
    Support Center