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nsv7003490

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 201 SVs from 46 studies. See in: genome view    
    Submitted genomic41,464,501-41,503,500Question Mark
    Overlapping variant regions from other studies: 70 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):33,540-72,539Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7003490Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1941,464,50141,503,500
    nsv7003490RemappedPerfectGRCh37.p13PATCHESFirst PassNW_004775434.1Chr19|NW_0
    04775434.1
    33,54072,539

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18425092deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18425092Submitted genomicNC_000019.10:g.414
    64501_41503500del
    GRCh38 (hg38)NC_000019.10Chr1941,464,50141,503,500
    nssv18425092RemappedPerfectNW_004775434.1:g.3
    3540_72539del
    GRCh37.p13First PassNW_004775434.1Chr19|NW_0
    04775434.1
    33,54072,539

    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)
    nssv184250920.002603255670
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