A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636313



Internal ID7023109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44817078..44825278hg38UCSC Ensembl
chr15:45109276..45117476hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg388201
hg198201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15233341, essv15233350, essv15233347, essv15233344, essv15233314, essv15233345, essv15233302, essv15233300, essv15233311, essv15233333, essv15233304, essv15233315, essv15233313, essv15233324, essv15233329, essv15233291, essv15233298, essv15233334, essv15233346, essv15233339, essv15233343, essv15233342, essv15233296, essv15233328, essv15233319, essv15233293, essv15233351, essv15233284, essv15233282, essv15233286, essv15233317, essv15233309, essv15233352, essv15233332, essv15233326, essv15233335, essv15233330, essv15233310, essv15233288, essv15233285, essv15233327, essv15233321, essv15233301, essv15233349, essv15233322, essv15233305, essv15233308, essv15233281, essv15233337, essv15233312, essv15233323, essv15233318, essv15233287, essv15233292, essv15233295, essv15233336, essv15233331, essv15233297, essv15233283, essv15233306, essv15233316, essv15233307, essv15233338, essv15233289, essv15233294, essv15233303, essv15233290, essv15233348, essv15233325, essv15233340, essv15233299, essv15233320
SamplesHG03366, NA19222, HG03121, HG02583, HG03163, NA19399, NA19332, HG03175, HG03111, NA19704, HG03515, HG02895, HG03133, HG03135, NA19307, HG03091, NA18923, HG03342, HG03578, NA19771, HG02054, NA20287, NA19404, NA19383, NA19137, NA19235, HG03195, HG02642, NA19385, NA19471, HG02946, HG03073, HG03394, NA19451, NA19200, HG02943, HG02439, NA19462, NA19152, NA19184, NA19327, HG03575, HG01345, HG03027, HG03294, HG01390, NA19449, HG03476, HG02577, NA19031, HG02884, NA19318, HG02586, HG01990, NA19401, NA19375, HG02667, NA19390, NA19321, NA18517, HG01272, HG03084, NA19328, HG02974, HG02095, HG03157, NA19472, HG02768, NA19213, NA18505, HG02808, HG03303
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636313
Frequency
Sample Size2504
Observed Gain72
Observed Loss0
Observed Complex0
Frequencyn/a


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