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nsv6610798

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,154

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 26 studies. See in: genome view    
    Submitted genomic39,763,661-39,764,814Question Mark
    Overlapping variant regions from other studies: 100 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):39,803,260-39,804,413Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6610798Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr739,763,66139,764,814
    nsv6610798RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr739,803,26039,804,413

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18156804deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18156804Submitted genomicNC_000007.14:g.397
    63661_39764814del
    GRCh38 (hg38)NC_000007.14Chr739,763,66139,764,814
    nssv18156804RemappedPerfectNC_000007.13:g.398
    03260_39804413del
    GRCh37.p13First PassNC_000007.13Chr739,803,26039,804,413

    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)
    nssv18156804<0.001937736
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