A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624418



Internal ID7011274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103548266..103551296hg38UCSC Ensembl
chr10:105308023..105311053hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg383031
hg193031
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13914669, essv13914640, essv13914661, essv13914638, essv13914675, essv13914673, essv13914668, essv13914662, essv13914664, essv13914684, essv13914642, essv13914633, essv13914676, essv13914639, essv13914649, essv13914667, essv13914635, essv13914657, essv13914630, essv13914671, essv13914663, essv13914641, essv13914645, essv13914651, essv13914632, essv13914636, essv13914658, essv13914643, essv13914654, essv13914631, essv13914670, essv13914678, essv13914683, essv13914634, essv13914652, essv13914648, essv13914646, essv13914680, essv13914682, essv13914666, essv13914647, essv13914653, essv13914629, essv13914650, essv13914677, essv13914659, essv13914681, essv13914655, essv13914672, essv13914679, essv13914665, essv13914644, essv13914674, essv13914637, essv13914660, essv13914656
SamplesNA19394, HG02890, NA19399, HG03175, HG02433, NA20321, HG03298, HG02476, HG03455, HG03295, NA20332, NA20346, NA18870, HG03133, HG01492, HG01083, NA20287, HG03267, HG03114, NA18867, HG00543, NA19403, NA19184, HG02449, NA20126, HG02555, HG03311, HG01390, HG03301, NA19114, HG03136, NA19031, NA19099, NA19318, HG02332, HG02896, HG03109, HG02330, NA19206, NA19321, HG03367, HG01915, HG03117, NA19331, NA20351, NA19334, HG03433, HG03127, HG02558, NA19328, HG02095, HG01912, NA19351, NA19146, NA18511, HG03198
Known GenesNEURL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624418
Frequency
Sample Size2504
Observed Gain56
Observed Loss0
Observed Complex0
Frequencyn/a


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