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nsv6900450

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:601,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1228 SVs from 77 studies. See in: genome view    
    Submitted genomic11,953,901-12,555,400Question Mark
    Overlapping variant regions from other studies: 1228 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):11,975,448-12,576,947Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6900450Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1111,953,90112,555,400
    nsv6900450RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1111,975,44812,576,947

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18575792duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18575792Submitted genomicNC_000011.10:g.119
    53901_12555400dup
    GRCh38 (hg38)NC_000011.10Chr1111,953,90112,555,400
    nssv18575792RemappedPerfectNC_000011.9:g.1197
    5448_12576947dup
    GRCh37.p13First PassNC_000011.9Chr1111,975,44812,576,947

    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)
    nssv185757924e-061275558
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