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nsv6335182

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:339

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 14 studies. See in: genome view    
    Submitted genomic94,310,961-94,311,299Question Mark
    Overlapping variant regions from other studies: 112 SVs from 14 studies. See in: genome view    
    Remapped(Score: Perfect):94,776,517-94,776,855Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6335182Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr194,310,96194,311,299
    nsv6335182RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr194,776,51794,776,855

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18065624deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18065624Submitted genomicNC_000001.11:g.943
    10961_94311299del
    GRCh38 (hg38)NC_000001.11Chr194,310,96194,311,299
    nssv18065624RemappedPerfectNC_000001.10:g.947
    76517_94776855del
    GRCh37.p13First PassNC_000001.10Chr194,776,51794,776,855

    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)
    nssv180656240.0014738674
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