U.S. flag

An official website of the United States government

nsv7042332

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:128,435

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 416 SVs from 47 studies. See in: genome view    
    Submitted genomic168,444,570-168,573,004Question Mark
    Overlapping variant regions from other studies: 416 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):167,871,575-168,000,009Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7042332Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5168,444,570168,573,004
    nsv7042332RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5167,871,575168,000,009

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18776125inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18776125Submitted genomicNC_000005.10:g.168
    444570_168573004in
    v
    GRCh38 (hg38)NC_000005.10Chr5168,444,570168,573,004
    nssv18776125RemappedPerfectNC_000005.9:g.1678
    71575_168000009inv
    GRCh37.p13First PassNC_000005.9Chr5167,871,575168,000,009

    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)
    nssv187761251.4e-054274096
    Support Center