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nsv6677615

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:83,126

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 604 SVs from 61 studies. See in: genome view    
    Submitted genomic43,817,923-43,901,048Question Mark
    Overlapping variant regions from other studies: 604 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):44,045,062-44,128,187Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6677615Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr243,817,92343,901,048
    nsv6677615RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr244,045,06244,128,187

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18664642duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18664642Submitted genomicNC_000002.12:g.438
    17923_43901048dup
    GRCh38 (hg38)NC_000002.12Chr243,817,92343,901,048
    nssv18664642RemappedPerfectNC_000002.11:g.440
    45062_44128187dup
    GRCh37.p13First PassNC_000002.11Chr244,045,06244,128,187

    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)
    nssv186646424e-061275528
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