A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627567



Internal ID7014395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103981074..103985752hg38UCSC Ensembl
chr11:103851802..103856480hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg384679
hg194679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14259639, essv14259591, essv14259592, essv14259640, essv14259613, essv14259603, essv14259629, essv14259611, essv14259610, essv14259601, essv14259634, essv14259630, essv14259604, essv14259642, essv14259626, essv14259633, essv14259631, essv14259595, essv14259614, essv14259594, essv14259635, essv14259596, essv14259622, essv14259623, essv14259605, essv14259619, essv14259641, essv14259624, essv14259625, essv14259636, essv14259627, essv14259612, essv14259621, essv14259637, essv14259616, essv14259606, essv14259638, essv14259615, essv14259602, essv14259632, essv14259597, essv14259618, essv14259628, essv14259600, essv14259609, essv14259620, essv14259607, essv14259593, essv14259617, essv14259598, essv14259608, essv14259599
SamplesHG01986, HG02339, HG02481, HG03163, HG03111, HG02433, NA19704, NA20332, HG03478, NA19171, NA18519, HG01070, HG03168, HG02485, HG01242, HG02281, NA19041, HG03189, NA19471, HG02420, HG03380, NA18908, HG02715, HG02477, HG03343, HG03120, HG02820, NA19908, HG01122, NA19462, HG03457, HG02757, HG03563, NA19449, HG03078, HG01890, NA19160, NA19149, HG03539, HG02546, NA19435, HG01396, NA19835, HG03127, HG02941, NA19310, HG02970, NA19468, NA19474, HG03351, NA19430, NA19312
Known GenesPDGFD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627567
Frequency
Sample Size2504
Observed Gain0
Observed Loss52
Observed Complex0
Frequencyn/a


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