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nsv7072716

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52,774

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 253 SVs from 44 studies. See in: genome view    
    Submitted genomic17,803,406-17,856,179Question Mark
    Overlapping variant regions from other studies: 49 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):232,197-284,970Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072716Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1017,803,40617,856,179
    nsv7072716RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003315932.1Chr10|NW_0
    03315932.1
    232,197284,970

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18731614inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18731614Submitted genomicNC_000010.11:g.178
    03406_17856179inv
    GRCh38 (hg38)NC_000010.11Chr1017,803,40617,856,179
    nssv18731614RemappedPerfectNW_003315932.1:g.2
    32197_284970inv
    GRCh37.p13First PassNW_003315932.1Chr10|NW_0
    03315932.1
    232,197284,970

    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)
    nssv187316141.4e-054273866
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