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nsv7146166

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):79,020,191-79,020,240Question Mark
    Overlapping variant regions from other studies: 125 SVs from 30 studies. See in: genome view    
    Submitted genomic79,486,534-79,486,583Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7146166RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1479,020,19179,020,240
    nsv7146166Submitted genomicGRCh37.p13Primary AssemblyNC_000014.8Chr1479,486,53479,486,583

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18838538deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18838538RemappedPerfectNC_000014.9:g.7902
    0191_79020240del
    GRCh38.p12First PassNC_000014.9Chr1479,020,19179,020,240
    nssv18838538Submitted genomicNC_000014.8:g.7948
    6534_79486583del
    GRCh37.p13NC_000014.8Chr1479,486,53479,486,583

    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)
    nssv188385380.512
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