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nsv6490999

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:290

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 87 SVs from 25 studies. See in: genome view    
    Submitted genomic116,871,162-116,871,451Question Mark
    Overlapping variant regions from other studies: 87 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):117,308,967-117,309,256Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6490999Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12116,871,162116,871,451
    nsv6490999RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12117,308,967117,309,256

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17997173deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17997173Submitted genomicNC_000012.12:g.116
    871162_116871451de
    l
    GRCh38 (hg38)NC_000012.12Chr12116,871,162116,871,451
    nssv17997173RemappedPerfectNC_000012.11:g.117
    308967_117309256de
    l
    GRCh37.p13First PassNC_000012.11Chr12117,308,967117,309,256

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv179971730.00414038994
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