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nsv6995685

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:41,105

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 245 SVs from 38 studies. See in: genome view    
    Submitted genomic44,244,895-44,285,999Question Mark
    Overlapping variant regions from other studies: 243 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):42,322,263-42,363,367Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6995685Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1744,244,89544,285,999
    nsv6995685RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1742,322,26342,363,367

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18412284deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18412284Submitted genomicNC_000017.11:g.442
    44895_44285999del
    GRCh38 (hg38)NC_000017.11Chr1744,244,89544,285,999
    nssv18412284RemappedPerfectNC_000017.10:g.423
    22263_42363367del
    GRCh37.p13First PassNC_000017.10Chr1742,322,26342,363,367

    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)
    nssv184122847e-062275888
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