A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1960e212



Internal ID22784887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130711653..130714934hg38UCSC Ensembl
chr7:130396482..130399762hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg383282
hg193281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3572143, esv3572144, esv3572145
Samples400287BP, 400570RW, 400618GC, 401196CR, 400439IM, 400094RS, 400626FC, 401460LW, 401972BA, 401491BB, 401845MJ, 400325BE, 400641WJ, 400675HC, 400588BE, 401104DM, 401746WW, 402056KD, 401997HB, 400107MJ, 401646MC, 401234MB, 400793BR, 401050GS, 400302HW, 400974PS, 401870FB, 400110MD, 400955BE, 401617KM, 401589HP, 400240HJ, 401357MH, 401825TH, 401419SW, 400724CD, 400705KK, 400846MC, 401580CA, 400319HT, 400354TJ, 401778CB, 400474GF, 400788PV, 400624RJ, 401496SL, 400770MA, 400483DP, 400881GS, 401611CD, 401149VA, 400971MK, 400586RD, 401166WJ, 401809FU, 400323AA, 401154BR, 400661AD, 400012CJ, 401510DG
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)dgv1960e212
Frequency
Sample Size873
Observed Gain0
Observed Loss60
Observed Complex0
Frequencyn/a


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