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nsv6503497

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,004

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 269 SVs from 49 studies. See in: genome view    
    Submitted genomic41,088,943-41,108,946Question Mark
    Overlapping variant regions from other studies: 267 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):39,245,195-39,265,198Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6503497Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1741,088,94341,108,946
    nsv6503497RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1739,245,19539,265,198

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18035459deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18035459Submitted genomicNC_000017.11:g.410
    88943_41108946del
    GRCh38 (hg38)NC_000017.11Chr1741,088,94341,108,946
    nssv18035459RemappedPerfectNC_000017.10:g.392
    45195_39265198del
    GRCh37.p13First PassNC_000017.10Chr1739,245,19539,265,198

    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)
    nssv18035459<0.0012938664
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