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nsv6931747

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 25 studies. See in: genome view    
    Submitted genomic62,297,399-62,299,198Question Mark
    Overlapping variant regions from other studies: 118 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):62,691,180-62,692,979Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6931747Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1262,297,39962,299,198
    nsv6931747RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1262,691,18062,692,979

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18371656deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18371656Submitted genomicNC_000012.12:g.622
    97399_62299198del
    GRCh38 (hg38)NC_000012.12Chr1262,297,39962,299,198
    nssv18371656RemappedPerfectNC_000012.11:g.626
    91180_62692979del
    GRCh37.p13First PassNC_000012.11Chr1262,691,18062,692,979

    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)
    nssv183716561.8e-055271360
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