U.S. flag

An official website of the United States government

nsv6425909

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,312

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 215 SVs from 38 studies. See in: genome view    
    Submitted genomic142,558,760-142,562,071Question Mark
    Overlapping variant regions from other studies: 110 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):742,523-745,834Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6425909Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7142,558,760142,562,071
    nsv6425909RemappedPerfectGRCh37.p13PATCHESSecond PassNW_003571040.1Chr7|NW_00
    3571040.1
    742,523745,834

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18217344duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18217344Submitted genomicNC_000007.14:g.142
    558760_142562071du
    p
    GRCh38 (hg38)NC_000007.14Chr7142,558,760142,562,071
    nssv18217344RemappedPerfectNW_003571040.1:g.7
    42523_745834dup
    GRCh37.p13Second PassNW_003571040.1Chr7|NW_00
    3571040.1
    742,523745,834

    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)
    nssv18217344<0.001539046
    Support Center