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nsv7006968

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:346,707

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2110 SVs from 101 studies. See in: genome view    
    Submitted genomic52,599,659-52,946,365Question Mark
    Overlapping variant regions from other studies: 2110 SVs from 101 studies. See in: genome view    
    Remapped(Score: Perfect):53,102,912-53,449,618Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7006968Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1952,599,65952,946,365
    nsv7006968RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1953,102,91253,449,618

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18636571duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18636571Submitted genomicNC_000019.10:g.525
    99659_52946365dup
    GRCh38 (hg38)NC_000019.10Chr1952,599,65952,946,365
    nssv18636571RemappedPerfectNC_000019.9:g.5310
    2912_53449618dup
    GRCh37.p13First PassNC_000019.9Chr1953,102,91253,449,618

    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)
    nssv186365713.3e-059270512
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