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nsv7145863

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:49

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 189 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):169,505,959-169,506,007Question Mark
    Overlapping variant regions from other studies: 189 SVs from 32 studies. See in: genome view    
    Submitted genomic170,362,469-170,362,517Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7145863RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2169,505,959169,506,007
    nsv7145863Submitted genomicGRCh37.p13Primary AssemblyNC_000002.11Chr2170,362,469170,362,517

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18841128deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18841128RemappedPerfectNC_000002.12:g.169
    505959_169506007de
    l
    GRCh38.p12First PassNC_000002.12Chr2169,505,959169,506,007
    nssv18841128Submitted genomicNC_000002.11:g.170
    362469_170362517de
    l
    GRCh37.p13NC_000002.11Chr2170,362,469170,362,517

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv188411280.524
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