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nsv6964633

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 32 studies. See in: genome view    
    Submitted genomic82,261,701-82,266,500Question Mark
    Overlapping variant regions from other studies: 152 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):82,554,042-82,558,841Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6964633Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1582,261,70182,266,500
    nsv6964633RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1582,554,04282,558,841

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18620611duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18620611Submitted genomicNC_000015.10:g.822
    61701_82266500dup
    GRCh38 (hg38)NC_000015.10Chr1582,261,70182,266,500
    nssv18620611RemappedPerfectNC_000015.9:g.8255
    4042_82558841dup
    GRCh37.p13First PassNC_000015.9Chr1582,554,04282,558,841

    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)
    nssv186206113.2e-059273222
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