A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638362



Internal ID7025148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29401122..29419575hg38UCSC Ensembl
chr16:29412443..29430896hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3818454
hg1918454
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15441451, essv15441426, essv15441477, essv15441474, essv15441446, essv15441476, essv15441428, essv15441481, essv15441486, essv15441498, essv15441489, essv15441453, essv15441467, essv15441432, essv15441435, essv15441501, essv15441473, essv15441471, essv15441458, essv15441504, essv15441442, essv15441439, essv15441503, essv15441469, essv15441462, essv15441488, essv15441480, essv15441487, essv15441441, essv15441506, essv15441419, essv15441484, essv15441465, essv15441463, essv15441460, essv15441440, essv15441433, essv15441494, essv15441482, essv15441417, essv15441429, essv15441485, essv15441456, essv15441468, essv15441457, essv15441466, essv15441475, essv15441455, essv15441422, essv15441414, essv15441459, essv15441415, essv15441493, essv15441470, essv15441421, essv15441478, essv15441450, essv15441444, essv15441425, essv15441443, essv15441447, essv15441479, essv15441436, essv15441491, essv15441452, essv15441431, essv15441483, essv15441505, essv15441496, essv15441424, essv15441416, essv15441438, essv15441472, essv15441427, essv15441449, essv15441502, essv15441497, essv15441495, essv15441500, essv15441492, essv15441437, essv15441461, essv15441464, essv15441420, essv15441454, essv15441490, essv15441430, essv15441423, essv15441499, essv15441445, essv15441413, essv15441434, essv15441418, essv15441448, essv15441412
SamplesNA18502, NA19701, HG03773, NA19028, HG02658, HG01441, HG03366, HG03121, NA19399, HG03687, HG02804, HG03190, NA20805, HG01456, NA18606, HG03139, HG03172, HG02888, HG02589, NA20356, HG02895, HG03099, NA18489, HG03091, HG02541, HG03485, HG02645, HG02054, HG03224, NA20287, HG03079, HG02143, HG03189, NA19917, NA19238, NA19172, HG02471, HG02588, HG03073, HG02623, HG02477, NA19027, HG00313, HG02442, HG03120, HG02977, HG03054, NA19437, HG01384, HG02380, HG02678, HG04162, HG02322, NA18915, HG03775, HG01345, HG02878, HG01049, HG03136, HG01197, NA19031, HG02884, HG02724, NA19318, HG03755, NA20296, NA19308, HG03028, NA11881, NA19108, NA18517, NA20276, HG03692, HG02837, NA19835, HG01620, HG03419, HG03703, HG03103, NA19328, NA19117, HG04140, HG03097, HG03049, NA19096, NA19121, HG03445, HG03376, HG03072, HG02805, HG03198, HG02629, HG02643, NA19153, NA19431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638362
Frequency
Sample Size2504
Observed Gain95
Observed Loss0
Observed Complex0
Frequencyn/a


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