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nsv7072980

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,637,381

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4033 SVs from 96 studies. See in: genome view    
    Submitted genomic102,790,775-104,428,155Question Mark
    Overlapping variant regions from other studies: 4033 SVs from 96 studies. See in: genome view    
    Remapped(Score: Perfect):103,803,003-105,440,383Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072980Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8102,790,775104,428,155
    nsv7072980RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8103,803,003105,440,383

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18781760inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18781760Submitted genomicNC_000008.11:g.102
    790775_104428155in
    v
    GRCh38 (hg38)NC_000008.11Chr8102,790,775104,428,155
    nssv18781760RemappedPerfectNC_000008.10:g.103
    803003_105440383in
    v
    GRCh37.p13First PassNC_000008.10Chr8103,803,003105,440,383

    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)
    nssv187817604e-061276268
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