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nsv6978614

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:69

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 16 studies. See in: genome view    
    Submitted genomic76,038,335-76,038,403Question Mark
    Overlapping variant regions from other studies: 134 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):74,034,416-74,034,484Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6978614Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1776,038,33576,038,403
    nsv6978614RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1774,034,41674,034,484

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631348duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631348Submitted genomicNC_000017.11:g.760
    38335_76038403dup
    GRCh38 (hg38)NC_000017.11Chr1776,038,33576,038,403
    nssv18631348RemappedPerfectNC_000017.10:g.740
    34416_74034484dup
    GRCh37.p13First PassNC_000017.10Chr1774,034,41674,034,484

    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)
    nssv186313485.9e-0513217572
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