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nsv6897765

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,950

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 22 studies. See in: genome view    
    Submitted genomic87,747,629-87,749,578Question Mark
    Overlapping variant regions from other studies: 117 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):89,507,386-89,509,335Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6897765Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1087,747,62987,749,578
    nsv6897765RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1089,507,38689,509,335

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18340740deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18340740Submitted genomicNC_000010.11:g.877
    47629_87749578del
    GRCh38 (hg38)NC_000010.11Chr1087,747,62987,749,578
    nssv18340740RemappedPerfectNC_000010.10:g.895
    07386_89509335del
    GRCh37.p13First PassNC_000010.10Chr1089,507,38689,509,335

    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)
    nssv18340740<0.001260272798
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