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nsv4593439

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:43,906

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 243 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):26,017,575-26,061,480Question Mark
    Overlapping variant regions from other studies: 243 SVs from 50 studies. See in: genome view    
    Submitted genomic26,017,803-26,061,708Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
    nsv4593439RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr626,017,57526,061,480
    nsv4593439Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr626,017,80326,061,708

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv16116778duplicationCuratedCurated

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
    nssv16116778RemappedPerfectNC_000006.12:g.(?_
    26017575)_(2606148
    0_?)dup    		GRCh38.p12First PassNC_000006.12Chr626,017,57526,061,480
    nssv16116778Submitted genomicNC_000006.11:g.(?_
    26017803)_(2606170
    8_?)dup    		GRCh37 (hg19)NC_000006.11Chr626,017,80326,061,708

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv161167780.0043845
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