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nsv6329133

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:551

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 124 SVs from 19 studies. See in: genome view    
    Submitted genomic43,701,909-43,702,459Question Mark
    Overlapping variant regions from other studies: 124 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):44,167,580-44,168,130Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6329133Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr143,701,90943,702,459
    nsv6329133RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr144,167,58044,168,130

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18061360deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18061360Submitted genomicNC_000001.11:g.437
    01909_43702459del
    GRCh38 (hg38)NC_000001.11Chr143,701,90943,702,459
    nssv18061360RemappedPerfectNC_000001.10:g.441
    67580_44168130del
    GRCh37.p13First PassNC_000001.10Chr144,167,58044,168,130

    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)
    nssv18061360<0.001134738
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