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nsv6886379

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:40,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 213 SVs from 33 studies. See in: genome view    
    Submitted genomic87,730,201-87,770,900Question Mark
    Overlapping variant regions from other studies: 213 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):89,489,958-89,530,657Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6886379Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1087,730,20187,770,900
    nsv6886379RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1089,489,95889,530,657

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18340739deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18340739Submitted genomicNC_000010.11:g.877
    30201_87770900del
    GRCh38 (hg38)NC_000010.11Chr1087,730,20187,770,900
    nssv18340739RemappedPerfectNC_000010.10:g.894
    89958_89530657del
    GRCh37.p13First PassNC_000010.10Chr1089,489,95889,530,657

    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)
    nssv183407394e-061276130
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