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nsv7042166

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,838

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 290 SVs from 56 studies. See in: genome view    
    Submitted genomic179,632,114-179,653,951Question Mark
    Overlapping variant regions from other studies: 290 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):179,059,115-179,080,952Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7042166Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5179,632,114179,653,951
    nsv7042166RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5179,059,115179,080,952

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775911inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775911Submitted genomicNC_000005.10:g.179
    632114_179653951in
    v
    GRCh38 (hg38)NC_000005.10Chr5179,632,114179,653,951
    nssv18775911RemappedPerfectNC_000005.9:g.1790
    59115_179080952inv
    GRCh37.p13First PassNC_000005.9Chr5179,059,115179,080,952

    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)
    nssv187759114e-061276268
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