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nsv7066269

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:92,064

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 269 SVs from 45 studies. See in: genome view    
    Submitted genomic17,800,810-17,892,873Question Mark
    Overlapping variant regions from other studies: 56 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):229,601-321,664Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066269Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1017,800,81017,892,873
    nsv7066269RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003315932.1Chr10|NW_0
    03315932.1
    229,601321,664

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18749731inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18749731Submitted genomicNC_000010.11:g.178
    00810_17892873inv
    GRCh38 (hg38)NC_000010.11Chr1017,800,81017,892,873
    nssv18749731RemappedPerfectNW_003315932.1:g.2
    29601_321664inv
    GRCh37.p13First PassNW_003315932.1Chr10|NW_0
    03315932.1
    229,601321,664

    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)
    nssv187497317e-062274964
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