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nsv7064007

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,941

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 201 SVs from 23 studies. See in: genome view    
    Submitted genomic106,553,348-106,563,288Question Mark
    Overlapping variant regions from other studies: 201 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):107,205,696-107,215,636Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064007Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13106,553,348106,563,288
    nsv7064007RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13107,205,696107,215,636

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752071inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752071Submitted genomicNC_000013.11:g.106
    553348_106563288in
    v
    GRCh38 (hg38)NC_000013.11Chr13106,553,348106,563,288
    nssv18752071RemappedPerfectNC_000013.10:g.107
    205696_107215636in
    v
    GRCh37.p13First PassNC_000013.10Chr13107,205,696107,215,636

    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)
    nssv187520714e-061276268
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