nsv5195742

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 200 SVs from 19 studies. See in: genome view    
    Submitted genomic123,516,395-123,516,400Question Mark
    Overlapping variant regions from other studies: 200 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):124,528,635-124,528,640Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv5195742Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8123,516,395123,516,400
    nsv5195742RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8124,528,635124,528,640

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv16666597line1 insertionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv16666597Submitted genomicNC_000008.11:g.123
    516395_123516400in
    s2119
    GRCh38 (hg38)NC_000008.11Chr8123,516,395123,516,400
    nssv16666597RemappedPerfectNC_000008.10:g.124
    528635_124528640in
    s2119
    GRCh37.p13First PassNC_000008.10Chr8124,528,635124,528,640

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Genotype Information

    Variant Call IDAllele Frequency (AF)
    nssv166665970.522
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