U.S. flag

An official website of the United States government

nsv6553867

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:750

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 123 SVs from 16 studies. See in: genome view    
    Submitted genomic200,780,316-200,781,065Question Mark
    Overlapping variant regions from other studies: 123 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):201,645,039-201,645,788Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6553867Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2200,780,316200,781,065
    nsv6553867RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2201,645,039201,645,788

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18256353inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18256353Submitted genomicNC_000002.12:g.200
    780316_200781065in
    v
    GRCh38 (hg38)NC_000002.12Chr2200,780,316200,781,065
    nssv18256353RemappedPerfectNC_000002.11:g.201
    645039_201645788in
    v
    GRCh37.p13First PassNC_000002.11Chr2201,645,039201,645,788

    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)
    nssv18256353<0.001135748
    Support Center