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nsv6971064

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:102,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 363 SVs from 45 studies. See in: genome view    
    Submitted genomic101,928,101-102,030,100Question Mark
    Overlapping variant regions from other studies: 363 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):102,394,438-102,496,437Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6971064Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr14101,928,101102,030,100
    nsv6971064RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr14102,394,438102,496,437

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18612834duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18612834Submitted genomicNC_000014.9:g.1019
    28101_102030100dup
    GRCh38 (hg38)NC_000014.9Chr14101,928,101102,030,100
    nssv18612834RemappedPerfectNC_000014.8:g.1023
    94438_102496437dup
    GRCh37.p13First PassNC_000014.8Chr14102,394,438102,496,437

    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)
    nssv186128344e-061274488
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