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nsv6887185

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:165,559

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 502 SVs from 56 studies. See in: genome view    
    Submitted genomic87,697,646-87,863,204Question Mark
    Overlapping variant regions from other studies: 502 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):89,457,403-89,622,961Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6887185Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1087,697,64687,863,204
    nsv6887185RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1089,457,40389,622,961

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18586179duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18586179Submitted genomicNC_000010.11:g.876
    97646_87863204dup
    GRCh38 (hg38)NC_000010.11Chr1087,697,64687,863,204
    nssv18586179RemappedPerfectNC_000010.10:g.894
    57403_89622961dup
    GRCh37.p13First PassNC_000010.10Chr1089,457,40389,622,961

    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)
    nssv185861794e-061275702
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