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nsv6791753

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:38,965

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 229 SVs from 49 studies. See in: genome view    
    Submitted genomic178,182,342-178,221,306Question Mark
    Overlapping variant regions from other studies: 229 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):177,609,343-177,648,307Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6791753Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5178,182,342178,221,306
    nsv6791753RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5177,609,343177,648,307

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18701452duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18701452Submitted genomicNC_000005.10:g.178
    182342_178221306du
    p
    GRCh38 (hg38)NC_000005.10Chr5178,182,342178,221,306
    nssv18701452RemappedPerfectNC_000005.9:g.1776
    09343_177648307dup
    GRCh37.p13First PassNC_000005.9Chr5177,609,343177,648,307

    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)
    nssv187014524e-061275218
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