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nsv6936182

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,918

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 130 SVs from 25 studies. See in: genome view    
    Submitted genomic29,207,232-29,211,149Question Mark
    Overlapping variant regions from other studies: 130 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):29,360,165-29,364,082Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6936182Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1229,207,23229,211,149
    nsv6936182RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1229,360,16529,364,082

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18360817deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18360817Submitted genomicNC_000012.12:g.292
    07232_29211149del
    GRCh38 (hg38)NC_000012.12Chr1229,207,23229,211,149
    nssv18360817RemappedPerfectNC_000012.11:g.293
    60165_29364082del
    GRCh37.p13First PassNC_000012.11Chr1229,360,16529,364,082

    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)
    nssv183608174e-061276242
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