A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645658



Internal ID7032407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31884362..31893992hg38UCSC Ensembl
chr20:30472165..30481795hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg389631
hg199631
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16173596, essv16173527, essv16173561, essv16173564, essv16173579, essv16173548, essv16173583, essv16173582, essv16173590, essv16173509, essv16173514, essv16173577, essv16173593, essv16173532, essv16173537, essv16173574, essv16173555, essv16173573, essv16173543, essv16173535, essv16173524, essv16173515, essv16173594, essv16173550, essv16173589, essv16173506, essv16173565, essv16173513, essv16173528, essv16173578, essv16173572, essv16173567, essv16173595, essv16173512, essv16173568, essv16173507, essv16173517, essv16173570, essv16173529, essv16173508, essv16173587, essv16173538, essv16173511, essv16173542, essv16173576, essv16173516, essv16173545, essv16173505, essv16173551, essv16173556, essv16173534, essv16173559, essv16173519, essv16173522, essv16173588, essv16173530, essv16173526, essv16173531, essv16173520, essv16173575, essv16173544, essv16173554, essv16173549, essv16173547, essv16173580, essv16173560, essv16173563, essv16173539, essv16173523, essv16173586, essv16173552, essv16173571, essv16173562, essv16173557, essv16173533, essv16173581, essv16173518, essv16173525, essv16173521, essv16173585, essv16173569, essv16173546, essv16173536, essv16173553, essv16173558, essv16173566, essv16173592, essv16173510, essv16173541, essv16173540, essv16173591, essv16173584
SamplesHG02614, HG02574, HG00114, HG01412, HG02702, NA20274, HG02433, NA19704, NA18507, HG03057, NA18881, HG02852, HG02836, HG02891, HG01305, NA20298, NA19819, HG03193, HG02769, HG02621, NA19201, HG02811, HG03168, HG02485, HG03091, HG03485, HG02315, NA18874, NA19917, HG02461, HG03045, NA19207, HG02471, HG03352, HG03225, HG02427, HG01198, NA19456, NA19027, HG03120, HG02334, HG02511, HG02449, HG02968, HG02757, HG02555, HG01102, HG01094, HG03563, HG03202, HG03397, NA19113, HG02881, HG02283, NA19095, HG02896, NA19625, HG02675, HG01896, NA20296, HG02613, NA19390, NA19108, NA18517, HG02759, HG03539, HG01915, HG02837, HG01260, HG02464, HG01108, NA20281, HG03419, HG03084, NA19117, NA18501, HG03565, NA20348, HG02974, NA19438, NA19472, HG01055, HG03063, HG03060, HG02676, HG03410, HG02679, NA18876, HG03538, HG03401, HG02947, HG02629
Known GenesTTLL9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645658
Frequency
Sample Size2504
Observed Gain92
Observed Loss0
Observed Complex0
Frequencyn/a


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