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nsv6663203

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:296

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 238 SVs from 46 studies. See in: genome view    
    Submitted genomic246,864,591-246,864,886Question Mark
    Overlapping variant regions from other studies: 241 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):247,027,893-247,028,188Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6663203Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1246,864,591246,864,886
    nsv6663203RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1247,027,893247,028,188

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18369133deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18369133Submitted genomicNC_000001.11:g.246
    864591_246864886de
    l
    GRCh38 (hg38)NC_000001.11Chr1246,864,591246,864,886
    nssv18369133RemappedPerfectNC_000001.10:g.247
    027893_247028188de
    l
    GRCh37.p13First PassNC_000001.10Chr1247,027,893247,028,188

    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)
    nssv183691330.716184962259366
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