A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1953e212



Internal ID22784880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116542041..116549717hg38UCSC Ensembl
chr7:116182095..116189771hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg387677
hg197677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3572092, esv3572093, esv3572095, esv3572094
Samples401474CE, 400247CL, 401806DL, 400599CP, 400618GC, 400987FB, 400802DP, 401592NR, 401235IA, 401117NA, 401927SK, 400449PK, 401151RJ, 401384BP, 401721CP, 400077EB, 400897MD, 400453LN, 400620MT, 400360SM, 401634CH, 400893ZE, 401064FR, 401975VD, 400827MM, 401924ST, 402028BD, 401869BG, 401006ES, 400134WK, 400526DR, 402012RR, 400579HJ, 400507VD, 401764JJ, 401873BK, 401437MJ, 400738WM, 401736BF, 401623SN, 401526WB, 400375KA, 401864CV, 401879HJ, 401630MK, 401262RR, 401017SC, 400006DK, 401812HG, 400639RP, 401067BD, 401039PA, 402074RR, 401259LS, 400030WD, 401677MM, 401334DH, 401391PJ, 401496SL, 400267GD, 400128MJ, 400996MC, 401372RR, 400106PC, 401781SL, 401354KM, 401177SL, 401932GN, 401395OP, 400782IE
Known GenesCAV1
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)dgv1953e212
Frequency
Sample Size873
Observed Gain0
Observed Loss70
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer