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nsv6968395

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,230

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 168 SVs from 37 studies. See in: genome view    
    Submitted genomic45,113,195-45,145,424Question Mark
    Overlapping variant regions from other studies: 168 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):45,405,393-45,437,622Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6968395Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1545,113,19545,145,424
    nsv6968395RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1545,405,39345,437,622

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18615656duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18615656Submitted genomicNC_000015.10:g.451
    13195_45145424dup
    GRCh38 (hg38)NC_000015.10Chr1545,113,19545,145,424
    nssv18615656RemappedPerfectNC_000015.9:g.4540
    5393_45437622dup
    GRCh37.p13First PassNC_000015.9Chr1545,405,39345,437,622

    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)
    nssv186156564e-061276004
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