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nsv6540096

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:562

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 152 SVs from 44 studies. See in: genome view    
    Submitted genomic113,602,734-113,603,295Question Mark
    Overlapping variant regions from other studies: 152 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):114,360,311-114,360,872Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6540096Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2113,602,734113,603,295
    nsv6540096RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2114,360,311114,360,872

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18256536inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18256536Submitted genomicNC_000002.12:g.113
    602734_113603295in
    v
    GRCh38 (hg38)NC_000002.12Chr2113,602,734113,603,295
    nssv18256536RemappedPerfectNC_000002.11:g.114
    360311_114360872in
    v
    GRCh37.p13First PassNC_000002.11Chr2114,360,311114,360,872

    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)
    nssv18256536<0.0011732536
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