A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607846



Internal ID6994777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:305181..340601hg38UCSC Ensembl
chr6:305181..340601hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3835421
hg1935421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1158e214
Supporting Variantsessv12164513, essv12164477, essv12164529, essv12164497, essv12164466, essv12164474, essv12164463, essv12164494, essv12164521, essv12164465, essv12164517, essv12164493, essv12164484, essv12164516, essv12164515, essv12164507, essv12164473, essv12164496, essv12164462, essv12164478, essv12164508, essv12164505, essv12164467, essv12164492, essv12164523, essv12164501, essv12164490, essv12164482, essv12164464, essv12164459, essv12164486, essv12164518, essv12164500, essv12164475, essv12164489, essv12164526, essv12164469, essv12164510, essv12164503, essv12164458, essv12164528, essv12164476, essv12164472, essv12164488, essv12164519, essv12164530, essv12164460, essv12164480, essv12164527, essv12164520, essv12164491, essv12164498, essv12164524, essv12164487, essv12164456, essv12164531, essv12164514, essv12164470, essv12164457, essv12164471, essv12164485, essv12164495, essv12164509, essv12164461, essv12164481, essv12164504, essv12164522, essv12164502, essv12164525, essv12164468, essv12164479, essv12164499, essv12164483, essv12164512, essv12164506, essv12164511
SamplesNA19701, HG01521, NA11829, HG04202, HG02419, NA20813, NA20802, HG03115, HG00318, HG03280, HG01686, HG00341, HG00654, HG02536, HG02285, NA18969, HG03086, HG02153, HG03757, NA20320, HG02541, HG01492, NA18916, HG02299, NA19197, NA12762, NA21108, HG03830, NA12761, HG00277, HG03897, HG00379, HG00705, NA19026, HG01932, HG00178, HG01605, HG00530, HG01603, HG02009, HG02402, NA18747, HG02136, NA19091, HG01595, HG02345, HG02380, HG01142, HG01607, HG01049, NA18536, NA12778, HG03991, HG00240, HG04200, NA18542, NA18952, HG02759, HG01362, HG00278, NA12873, HG01620, NA20544, NA20887, HG02181, HG00125, HG03600, HG02971, HG01917, HG01935, HG03733, HG01302, HG01111, HG03072, NA19065, HG03741
Known GenesDUSP22
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607846
Frequency
Sample Size2504
Observed Gain76
Observed Loss0
Observed Complex0
Frequencyn/a


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