A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640223



Internal ID6680310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20919982..20922460hg38UCSC Ensembl
Innerchr17:20919986..20922457hg38UCSC Ensembl
Outerchr17:20919979..20922464hg38UCSC Ensembl
chr17:20823295..20825773hg19UCSC Ensembl
Innerchr17:20823299..20825770hg19UCSC Ensembl
Outerchr17:20823292..20825777hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382479
hg192479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15650583, essv15650634, essv15650587, essv15650594, essv15650551, essv15650552, essv15650621, essv15650628, essv15650590, essv15650650, essv15650553, essv15650595, essv15650646, essv15650541, essv15650653, essv15650605, essv15650569, essv15650652, essv15650549, essv15650620, essv15650640, essv15650537, essv15650556, essv15650544, essv15650629, essv15650568, essv15650547, essv15650637, essv15650603, essv15650575, essv15650542, essv15650543, essv15650630, essv15650592, essv15650600, essv15650582, essv15650608, essv15650645, essv15650578, essv15650619, essv15650602, essv15650642, essv15650651, essv15650597, essv15650563, essv15650555, essv15650643, essv15650612, essv15650536, essv15650571, essv15650566, essv15650560, essv15650631, essv15650573, essv15650550, essv15650641, essv15650557, essv15650565, essv15650632, essv15650570, essv15650562, essv15650647, essv15650584, essv15650644, essv15650607, essv15650611, essv15650638, essv15650585, essv15650614, essv15650581, essv15650639, essv15650654, essv15650579, essv15650545, essv15650539, essv15650610, essv15650561, essv15650572, essv15650633, essv15650636, essv15650615, essv15650593, essv15650625, essv15650586, essv15650577, essv15650554, essv15650559, essv15650598, essv15650558, essv15650589, essv15650535, essv15650618, essv15650591, essv15650616, essv15650564, essv15650626, essv15650622, essv15650609, essv15650574, essv15650623, essv15650606, essv15650567, essv15650635, essv15650624, essv15650576, essv15650596, essv15650540, essv15650655, essv15650648, essv15650601, essv15650658, essv15650604, essv15650599, essv15650627, essv15650649, essv15650656, essv15650546, essv15650617, essv15650657, essv15650613, essv15650588, essv15650580, essv15650548, essv15650538
SamplesNA19028, HG03559, HG02890, NA19700, HG02481, NA19909, NA19378, HG03717, HG02852, HG02419, HG02798, HG03115, HG02891, HG03130, NA20298, HG03190, NA19393, NA19443, NA19098, NA18870, NA19314, HG03069, HG02895, NA19107, NA19446, HG03086, NA19319, HG03385, NA20756, HG02620, NA18916, HG02854, HG02054, HG01063, NA18498, HG03224, HG03040, HG02111, HG03209, HG01398, HG03189, NA18874, NA19917, NA19235, NA19159, NA19901, NA20127, NA18908, NA19451, HG02819, HG02943, HG02570, HG03054, HG03861, HG01187, NA18934, NA19152, NA18933, NA19984, HG02449, NA19913, NA20126, HG03081, HG02497, HG02470, HG03301, NA19114, HG01414, HG03476, HG03388, NA19031, NA18856, NA19740, NA19320, HG03024, NA19761, HG02586, HG02896, HG02722, NA19017, NA19375, HG03028, HG02667, NA19390, NA19256, HG02799, NA19473, NA19037, HG02923, NA19144, NA18865, NA19835, HG02982, HG03433, HG03127, HG02839, NA19360, HG02814, HG02558, NA19475, NA19143, HG03565, HG03039, NA20348, HG03442, NA19472, HG02646, HG03049, NA19468, HG03279, HG02938, HG03351, HG02768, NA19096, HG02051, HG01883, HG02763, NA19430, NA18505, NA19463, HG02808, HG03303, NA19346, NA19153
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640223
Frequency
Sample Size2504
Observed Gain0
Observed Loss124
Observed Complex0
Frequencyn/a


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