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nsv7146764

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 116 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):65,537,057-65,537,130Question Mark
    Overlapping variant regions from other studies: 116 SVs from 33 studies. See in: genome view    
    Submitted genomic65,570,960-65,571,033Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7146764RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1665,537,05765,537,130
    nsv7146764Submitted genomicGRCh37.p13Primary AssemblyNC_000016.9Chr1665,570,96065,571,033

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18840956deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18840956RemappedPerfectNC_000016.10:g.655
    37057_65537130del
    GRCh38.p12First PassNC_000016.10Chr1665,537,05765,537,130
    nssv18840956Submitted genomicNC_000016.9:g.6557
    0960_65571033del
    GRCh37.p13NC_000016.9Chr1665,570,96065,571,033

    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)
    nssv188409560.524
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