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nsv6889697

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,058

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 83 SVs from 18 studies. See in: genome view    
    Submitted genomic116,158,970-116,164,027Question Mark
    Overlapping variant regions from other studies: 83 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):117,918,482-117,923,539Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6889697Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10116,158,970116,164,027
    nsv6889697RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10117,918,482117,923,539

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18332134deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18332134Submitted genomicNC_000010.11:g.116
    158970_116164027de
    l
    GRCh38 (hg38)NC_000010.11Chr10116,158,970116,164,027
    nssv18332134RemappedPerfectNC_000010.10:g.117
    918482_117923539de
    l
    GRCh37.p13First PassNC_000010.10Chr10117,918,482117,923,539

    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)
    nssv183321344e-061276236
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