U.S. flag

An official website of the United States government

nsv7022955

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:158,462

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 626 SVs from 70 studies. See in: genome view    
    Submitted genomic41,175,146-41,333,607Question Mark
    Overlapping variant regions from other studies: 626 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):41,571,150-41,729,611Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7022955Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2241,175,14641,333,607
    nsv7022955RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2241,571,15041,729,611

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18653024duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18653024Submitted genomicNC_000022.11:g.411
    75146_41333607dup
    GRCh38 (hg38)NC_000022.11Chr2241,175,14641,333,607
    nssv18653024RemappedPerfectNC_000022.10:g.415
    71150_41729611dup
    GRCh37.p13First PassNC_000022.10Chr2241,571,15041,729,611

    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)
    nssv186530244e-061275712
    Support Center