U.S. flag

An official website of the United States government

nsv7054658

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,910,590

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6767 SVs from 111 studies. See in: genome view    
    Submitted genomic183,954,061-185,864,650Question Mark
    Overlapping variant regions from other studies: 6769 SVs from 111 studies. See in: genome view    
    Remapped(Score: Perfect):184,875,214-186,785,804Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054658Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4183,954,061185,864,650
    nsv7054658RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4184,875,214186,785,804

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18773984inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18773984Submitted genomicNC_000004.12:g.183
    954061_185864650in
    v
    GRCh38 (hg38)NC_000004.12Chr4183,954,061185,864,650
    nssv18773984RemappedPerfectNC_000004.11:g.184
    875214_186785804in
    v
    GRCh37.p13First PassNC_000004.11Chr4184,875,214186,785,804

    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)
    nssv187739844e-061276268
    Support Center