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nsv7072319

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,969,701

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8845 SVs from 116 studies. See in: genome view    
    Submitted genomic99,798,704-101,768,404Question Mark
    Overlapping variant regions from other studies: 8845 SVs from 116 studies. See in: genome view    
    Remapped(Score: Perfect):100,338,909-102,308,607Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072319Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1599,798,704101,768,404
    nsv7072319RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr15100,338,909102,308,607

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756779inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756779Submitted genomicNC_000015.10:g.997
    98704_101768404inv
    GRCh38 (hg38)NC_000015.10Chr1599,798,704101,768,404
    nssv18756779RemappedPerfectNC_000015.9:g.1003
    38909_102308607inv
    GRCh37.p13First PassNC_000015.9Chr15100,338,909102,308,607

    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)
    nssv187567794e-061276268
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