A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3630980



Internal ID6671113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122701033..122714056hg38UCSC Ensembl
chr12:123185580..123198603hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3813024
hg1913024
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14621544, essv14621536, essv14621532, essv14621543, essv14621467, essv14621489, essv14621526, essv14621501, essv14621530, essv14621521, essv14621520, essv14621486, essv14621497, essv14621468, essv14621514, essv14621458, essv14621519, essv14621463, essv14621541, essv14621529, essv14621498, essv14621527, essv14621524, essv14621523, essv14621495, essv14621471, essv14621455, essv14621483, essv14621537, essv14621484, essv14621515, essv14621454, essv14621482, essv14621545, essv14621465, essv14621466, essv14621528, essv14621511, essv14621464, essv14621456, essv14621500, essv14621490, essv14621534, essv14621487, essv14621510, essv14621525, essv14621477, essv14621503, essv14621522, essv14621507, essv14621539, essv14621469, essv14621473, essv14621531, essv14621512, essv14621505, essv14621533, essv14621475, essv14621459, essv14621493, essv14621546, essv14621499, essv14621496, essv14621460, essv14621509, essv14621508, essv14621462, essv14621488, essv14621518, essv14621506, essv14621470, essv14621540, essv14621538, essv14621481, essv14621480, essv14621494, essv14621502, essv14621476, essv14621472, essv14621474, essv14621504, essv14621457, essv14621478, essv14621513, essv14621516, essv14621485, essv14621461, essv14621491, essv14621535, essv14621492, essv14621517, essv14621542, essv14621479
SamplesHG00626, NA18998, NA18745, HG00442, NA19055, NA18621, NA18647, NA18592, HG00559, NA18561, NA18979, HG00457, NA18999, NA18596, NA18606, HG02154, HG00654, HG01704, NA18962, HG00693, NA18967, HG00622, NA19076, NA19379, NA18597, HG02690, HG03722, NA19762, NA18635, NA18942, NA19062, NA18574, NA18642, NA20768, NA12287, NA19054, HG01848, HG01372, NA19079, HG02131, NA18749, NA18970, HG00705, NA18973, NA18539, HG00108, HG02879, HG02047, HG00443, NA18538, NA19091, NA19070, HG00596, NA19006, HG01595, HG02513, NA19077, HG02380, NA18644, HG00436, HG00533, HG00598, HG00583, NA18948, HG00651, NA19000, HG01762, HG00404, HG00531, NA11894, NA18946, NA18532, HG00613, NA18555, HG00704, HG00463, NA18531, NA12546, HG01596, NA19012, HG01597, NA18564, NA18950, HG00623, NA18629, NA18643, NA18591, HG04003, HG00472, NA18740, HG01578, NA19074, HG00437
Known GenesHCAR2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3630980
Frequency
Sample Size2504
Observed Gain93
Observed Loss0
Observed Complex0
Frequencyn/a


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