U.S. flag

An official website of the United States government

nsv6908016

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,024

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 141 SVs from 35 studies. See in: genome view    
    Submitted genomic66,482,408-66,510,431Question Mark
    Overlapping variant regions from other studies: 141 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):66,249,879-66,277,902Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6908016Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1166,482,40866,510,431
    nsv6908016RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1166,249,87966,277,902

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18581066duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18581066Submitted genomicNC_000011.10:g.664
    82408_66510431dup
    GRCh38 (hg38)NC_000011.10Chr1166,482,40866,510,431
    nssv18581066RemappedPerfectNC_000011.9:g.6624
    9879_66277902dup
    GRCh37.p13First PassNC_000011.9Chr1166,249,87966,277,902

    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)
    nssv185810664e-061275618
    Support Center