A curated catalogue of human genomic structural variation

Variant Details

Variant: esv3630980

Internal ID6671113
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122701033..122714056hg38UCSC Ensembl
chr12:123185580..123198603hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14621479, essv14621537, essv14621487, essv14621477, essv14621543, essv14621456, essv14621492, essv14621501, essv14621461, essv14621541, essv14621466, essv14621540, essv14621526, essv14621486, essv14621539, essv14621533, essv14621463, essv14621513, essv14621544, essv14621515, essv14621497, essv14621545, essv14621495, essv14621506, essv14621490, essv14621519, essv14621542, essv14621528, essv14621474, essv14621482, essv14621511, essv14621516, essv14621462, essv14621496, essv14621531, essv14621509, essv14621517, essv14621514, essv14621534, essv14621510, essv14621500, essv14621508, essv14621504, essv14621484, essv14621491, essv14621473, essv14621521, essv14621488, essv14621454, essv14621522, essv14621458, essv14621460, essv14621530, essv14621481, essv14621485, essv14621471, essv14621457, essv14621467, essv14621472, essv14621505, essv14621518, essv14621525, essv14621476, essv14621532, essv14621478, essv14621493, essv14621507, essv14621524, essv14621529, essv14621520, essv14621523, essv14621512, essv14621502, essv14621464, essv14621455, essv14621475, essv14621468, essv14621499, essv14621535, essv14621494, essv14621470, essv14621489, essv14621465, essv14621538, essv14621503, essv14621469, essv14621483, essv14621498, essv14621480, essv14621459, essv14621536, essv14621546, essv14621527
SamplesNA18642, HG02879, HG00613, HG01372, NA19012, NA18621, NA18647, HG04003, NA18561, HG00705, HG00437, HG00596, HG00457, HG02513, NA18948, HG00463, NA18591, HG01704, NA19379, HG01762, HG00404, HG00651, HG01848, NA18745, NA12287, NA18950, HG02047, NA18596, HG01597, NA19077, NA19762, NA19062, NA18979, NA18998, NA18967, NA19054, NA19076, HG00472, HG00583, NA18635, HG01595, NA18644, NA18531, NA18592, HG00533, NA11894, NA18973, HG02380, NA18643, HG01596, HG03722, NA18970, NA18539, NA19000, NA19055, HG00436, HG02131, HG00108, HG00559, NA18749, NA18564, NA18942, NA19074, NA19091, HG02690, NA18606, NA18999, NA18597, HG00443, HG02154, NA18538, NA18740, HG00654, NA18946, NA12546, NA19006, NA19070, HG00623, HG00693, NA20768, NA18532, NA18574, HG00442, HG00598, NA19079, HG00626, HG00622, HG00704, NA18555, HG00531, NA18629, HG01578, NA18962
Known GenesHCAR2
PlatformMultiple platforms
Pubmed ID21293372
Accession Number(s)esv3630980
Sample Size2504
Observed Gain93
Observed Loss0
Observed Complex0

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