A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585356



Internal ID6625675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16936619..16947018hg38UCSC Ensembl
chr1:17263114..17273513hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv14e214
Supporting Variantsessv9874516, essv9874529, essv9874532, essv9874493, essv9874537, essv9874496, essv9874545, essv9874519, essv9874528, essv9874543, essv9874501, essv9874488, essv9874540, essv9874561, essv9874544, essv9874551, essv9874527, essv9874553, essv9874536, essv9874525, essv9874524, essv9874487, essv9874558, essv9874489, essv9874552, essv9874498, essv9874490, essv9874518, essv9874510, essv9874538, essv9874548, essv9874514, essv9874547, essv9874535, essv9874546, essv9874502, essv9874521, essv9874550, essv9874541, essv9874506, essv9874505, essv9874509, essv9874515, essv9874512, essv9874486, essv9874542, essv9874513, essv9874495, essv9874523, essv9874531, essv9874517, essv9874507, essv9874563, essv9874555, essv9874522, essv9874554, essv9874556, essv9874530, essv9874562, essv9874557, essv9874526, essv9874508, essv9874492, essv9874560, essv9874511, essv9874534, essv9874533, essv9874503, essv9874549, essv9874559, essv9874491, essv9874500, essv9874539, essv9874499, essv9874520, essv9874494, essv9874504, essv9874497
SamplesNA18745, HG01462, HG02318, NA18599, HG01066, HG02891, HG03130, NA19819, HG02888, NA20359, HG03133, HG00641, HG03464, HG01070, NA19319, HG01488, HG02840, NA19457, HG01063, NA18749, HG02703, HG02634, HG03225, NA19239, HG03267, HG03058, NA19445, NA20127, HG02479, HG01565, HG02716, HG02943, HG02442, HG02439, HG03054, HG03061, HG01790, NA19327, NA19455, HG02322, HG02450, HG03771, HG02817, HG03202, HG03446, HG02881, NA18853, NA20282, NA19099, NA19225, HG01286, NA19160, HG01990, NA19035, NA19206, NA19834, NA19712, HG02010, HG00353, HG02983, HG00375, NA07051, HG01174, HG03304, HG02317, NA19783, HG02814, HG00672, NA19248, NA19472, HG01783, NA19770, NA18876, NA19711, HG01775, HG03376, HG02808, HG01061
Known GenesCROCC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585356
Frequency
Sample Size2504
Observed Gain78
Observed Loss0
Observed Complex0
Frequencyn/a


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