A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619078



Internal ID7005959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142095814..142096276hg38UCSC Ensembl
Innerchr8:142095826..142096264hg38UCSC Ensembl
Outerchr8:142095802..142096288hg38UCSC Ensembl
chr8:143177175..143177637hg19UCSC Ensembl
Innerchr8:143177187..143177625hg19UCSC Ensembl
Outerchr8:143177163..143177649hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13361729, essv13361739, essv13361684, essv13361675, essv13361670, essv13361737, essv13361725, essv13361743, essv13361689, essv13361680, essv13361742, essv13361711, essv13361661, essv13361665, essv13361686, essv13361674, essv13361663, essv13361726, essv13361699, essv13361746, essv13361723, essv13361745, essv13361735, essv13361683, essv13361709, essv13361695, essv13361740, essv13361748, essv13361700, essv13361679, essv13361657, essv13361744, essv13361685, essv13361733, essv13361669, essv13361673, essv13361732, essv13361672, essv13361662, essv13361658, essv13361677, essv13361702, essv13361707, essv13361676, essv13361668, essv13361701, essv13361664, essv13361714, essv13361747, essv13361690, essv13361682, essv13361712, essv13361681, essv13361660, essv13361730, essv13361696, essv13361736, essv13361703, essv13361721, essv13361713, essv13361704, essv13361687, essv13361678, essv13361708, essv13361722, essv13361720, essv13361659, essv13361671, essv13361741, essv13361727, essv13361734, essv13361710, essv13361724, essv13361688, essv13361716, essv13361693, essv13361738, essv13361731, essv13361698, essv13361694, essv13361706, essv13361656, essv13361705, essv13361697, essv13361718, essv13361666, essv13361728, essv13361667, essv13361715, essv13361691, essv13361719, essv13361717, essv13361692
SamplesHG02574, HG03559, HG02944, HG02628, HG03121, HG03163, NA19914, NA19332, HG02702, NA19704, HG01188, NA19020, HG03558, NA19092, HG03521, NA20298, NA19819, HG03518, HG03139, HG01051, NA19314, HG03069, NA19446, NA19374, HG03436, NA18519, HG03452, NA19119, HG02756, NA19131, HG02860, HG02816, HG02489, HG03209, HG02561, HG01628, NA19172, HG03352, NA18520, NA20342, HG03169, HG03343, HG02820, HG02570, NA19908, HG03511, NA19462, HG02450, HG01989, NA18910, HG01880, HG02976, HG02878, HG03294, NA18907, HG03123, NA19042, NA19320, HG02256, HG01890, HG01403, HG03109, HG02675, NA19436, HG02455, HG02557, NA19147, NA19712, HG03539, HG02501, HG02010, NA19473, HG02983, NA19331, HG03259, NA19439, NA19428, HG03419, HG03108, NA19117, HG02974, NA19474, HG01055, NA19102, NA18873, NA19900, HG02051, HG01914, HG03445, HG02861, NA19346, NA19153, NA19431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619078
Frequency
Sample Size2504
Observed Gain0
Observed Loss93
Observed Complex0
Frequencyn/a


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