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nsv6435851

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:317

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 24 studies. See in: genome view    
    Submitted genomic94,093,924-94,094,240Question Mark
    Overlapping variant regions from other studies: 94 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):95,853,681-95,853,997Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6435851Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1094,093,92494,094,240
    nsv6435851RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1095,853,68195,853,997

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17985238deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17985238Submitted genomicNC_000010.11:g.940
    93924_94094240del
    GRCh38 (hg38)NC_000010.11Chr1094,093,92494,094,240
    nssv17985238RemappedPerfectNC_000010.10:g.958
    53681_95853997del
    GRCh37.p13First PassNC_000010.10Chr1095,853,68195,853,997

    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)
    nssv179852380.00922125716
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