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nsv6646424

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:147,999

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 596 SVs from 59 studies. See in: genome view    
    Submitted genomic19,486,193-19,634,191Question Mark
    Overlapping variant regions from other studies: 596 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):19,812,687-19,960,685Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6646424Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr119,486,19319,634,191
    nsv6646424RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr119,812,68719,960,685

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18607750duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18607750Submitted genomicNC_000001.11:g.194
    86193_19634191dup
    GRCh38 (hg38)NC_000001.11Chr119,486,19319,634,191
    nssv18607750RemappedPerfectNC_000001.10:g.198
    12687_19960685dup
    GRCh37.p13First PassNC_000001.10Chr119,812,68719,960,685

    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)
    nssv186077504e-061275844
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