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nsv7004613

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:60,581

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 335 SVs from 48 studies. See in: genome view    
    Submitted genomic49,212,131-49,272,711Question Mark
    Overlapping variant regions from other studies: 335 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):49,715,388-49,775,968Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7004613Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1949,212,13149,272,711
    nsv7004613RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,715,38849,775,968

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18640922duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18640922Submitted genomicNC_000019.10:g.492
    12131_49272711dup
    GRCh38 (hg38)NC_000019.10Chr1949,212,13149,272,711
    nssv18640922RemappedPerfectNC_000019.9:g.4971
    5388_49775968dup
    GRCh37.p13First PassNC_000019.9Chr1949,715,38849,775,968

    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)
    nssv186409227e-062275130
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