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nsv7072770

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:73

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 19 studies. See in: genome view    
    Submitted genomic17,877,710-17,877,782Question Mark
    Overlapping variant regions from other studies: 3 SVs from 3 studies. See in: genome view    
    Remapped(Score: Perfect):306,501-306,573Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072770Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1017,877,71017,877,782
    nsv7072770RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003315932.1Chr10|NW_0
    03315932.1
    306,501306,573

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18737417inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18737417Submitted genomicNC_000010.11:g.178
    77710_17877782inv
    GRCh38 (hg38)NC_000010.11Chr1017,877,71017,877,782
    nssv18737417RemappedPerfectNW_003315932.1:g.3
    06501_306573inv
    GRCh37.p13First PassNW_003315932.1Chr10|NW_0
    03315932.1
    306,501306,573

    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)
    nssv18737417<0.001131275180
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