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nsv6921571

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,916

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 37 studies. See in: genome view    
    Submitted genomic95,172,482-95,182,397Question Mark
    Overlapping variant regions from other studies: 119 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):95,566,258-95,576,173Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6921571Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1295,172,48295,182,397
    nsv6921571RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1295,566,25895,576,173

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18373666deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18373666Submitted genomicNC_000012.12:g.951
    72482_95182397del
    GRCh38 (hg38)NC_000012.12Chr1295,172,48295,182,397
    nssv18373666RemappedPerfectNC_000012.11:g.955
    66258_95576173del
    GRCh37.p13First PassNC_000012.11Chr1295,566,25895,576,173

    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)
    nssv183736667e-062275964
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