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nsv6995401

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,671

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 109 SVs from 25 studies. See in: genome view    
    Submitted genomic6,616,124-6,619,794Question Mark
    Overlapping variant regions from other studies: 109 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):6,519,444-6,523,114Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6995401Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr176,616,1246,619,794
    nsv6995401RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr176,519,4446,523,114

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18413521deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18413521Submitted genomicNC_000017.11:g.661
    6124_6619794del
    GRCh38 (hg38)NC_000017.11Chr176,616,1246,619,794
    nssv18413521RemappedPerfectNC_000017.10:g.651
    9444_6523114del
    GRCh37.p13First PassNC_000017.10Chr176,519,4446,523,114

    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)
    nssv184135214e-061276108
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