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nsv6440427

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:158,621

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 447 SVs from 54 studies. See in: genome view    
    Submitted genomic103,392,774-103,551,394Question Mark
    Overlapping variant regions from other studies: 447 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):105,152,531-105,311,151Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6440427Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10103,392,774103,551,394
    nsv6440427RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10105,152,531105,311,151

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18189042duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18189042Submitted genomicNC_000010.11:g.103
    392774_103551394du
    p
    GRCh38 (hg38)NC_000010.11Chr10103,392,774103,551,394
    nssv18189042RemappedPerfectNC_000010.10:g.105
    152531_105311151du
    p
    GRCh37.p13First PassNC_000010.10Chr10105,152,531105,311,151

    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)
    nssv18189042<0.001239286
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