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nsv4600325

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,206

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 88 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):96,519,847-96,521,052Question Mark
    Overlapping variant regions from other studies: 88 SVs from 24 studies. See in: genome view    
    Submitted genomic98,279,604-98,280,809Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
    nsv4600325RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1096,519,84796,521,052
    nsv4600325Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr1098,279,60498,280,809

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv16112866deletionCuratedCurated

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
    nssv16112866RemappedPerfectNC_000010.11:g.(?_
    96519847)_(9652105
    2_?)del
    GRCh38.p12First PassNC_000010.11Chr1096,519,84796,521,052
    nssv16112866Submitted genomicNC_000010.10:g.(?_
    98279604)_(9828080
    9_?)del
    GRCh37 (hg19)NC_000010.10Chr1098,279,60498,280,809

    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)
    nssv161128660.0011845
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