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nsv6564369

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:829

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
    Submitted genomic109,656,383-109,657,211Question Mark
    Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):110,577,539-110,578,367Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6564369Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4109,656,383109,657,211
    nsv6564369RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4110,577,539110,578,367

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18263559inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18263559Submitted genomicNC_000004.12:g.109
    656383_109657211in
    v
    GRCh38 (hg38)NC_000004.12Chr4109,656,383109,657,211
    nssv18263559RemappedPerfectNC_000004.11:g.110
    577539_110578367in
    v
    GRCh37.p13First PassNC_000004.11Chr4110,577,539110,578,367

    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)
    nssv18263559<0.001236774
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