A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv677e212



Internal ID22783604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103302365..103321249hg38UCSC Ensembl
chr14:103768702..103787586hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3818885
hg1918885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3581410, esv3581412, esv3581411, esv3581409
Samples401482CB, 401474CE, 401819BS, 400336BG, 401235IA, 401503MJ, 400574MA, 400068PW, 401151RJ, 401733CG, 400897MD, 401426WD, 401355CD, 400827MM, 402062KR, 400203NA, 401832MC, 400353ML, 400218WK, 401050GS, 400763BT, 401785MJ, 401432SB, 401419SW, 401606CG, 401940SJ, 401359HF, 400201PK, 401268PS, 400410CD, 401781SL, 400833BB, 401612HB, 400923OA
Known Genes
MethodSNP array
AnalysisWe used four separate algorithms to detect CNVs; Affymetrix Chromosome Analysis Suite (ChAS), iPattern, Nexus and Partek. Our primary analysis was performed based on ChAS CNV calls, which were then supported using the remaining three algorithms to construct a confidence set of CNVs. For all algorithms, we have used 8 probes and >1kb as a base line cutoff for CNV detection.
PlatformAffymetrix CytoScan HD 2.7M array
Comments
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)dgv677e212
Frequency
Sample Size873
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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