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nsv7060011

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:604,099

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1542 SVs from 75 studies. See in: genome view    
    Submitted genomic116,124,560-116,728,658Question Mark
    Overlapping variant regions from other studies: 1185 SVs from 69 studies. See in: genome view    
    Remapped(Score: Pass):117,884,071-118,348,516Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060011Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10116,124,560116,728,658
    nsv7060011RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10117,884,071118,348,516

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18748493inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18748493Submitted genomicNC_000010.11:g.116
    124560_116728658in
    v
    GRCh38 (hg38)NC_000010.11Chr10116,124,560116,728,658
    nssv18748493RemappedPassNC_000010.10:g.117
    884071_118348516in
    v
    GRCh37.p13First PassNC_000010.10Chr10117,884,071118,348,516

    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)
    nssv187484934e-061276268
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