A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635393



Internal ID7022192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94949356..94952521hg38UCSC Ensembl
chr14:95415693..95418858hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg383166
hg193166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103341, essv15103289, essv15103335, essv15103333, essv15103286, essv15103309, essv15103306, essv15103330, essv15103292, essv15103299, essv15103303, essv15103304, essv15103280, essv15103311, essv15103305, essv15103354, essv15103339, essv15103291, essv15103295, essv15103288, essv15103282, essv15103355, essv15103343, essv15103281, essv15103315, essv15103317, essv15103293, essv15103312, essv15103297, essv15103310, essv15103345, essv15103340, essv15103325, essv15103324, essv15103328, essv15103336, essv15103344, essv15103323, essv15103337, essv15103349, essv15103321, essv15103318, essv15103301, essv15103352, essv15103346, essv15103334, essv15103283, essv15103322, essv15103313, essv15103287, essv15103308, essv15103294, essv15103302, essv15103350, essv15103326, essv15103348, essv15103329, essv15103285, essv15103347, essv15103320, essv15103351, essv15103332, essv15103316, essv15103327, essv15103300, essv15103353, essv15103279, essv15103331, essv15103342, essv15103307, essv15103314, essv15103290, essv15103298, essv15103338, essv15103284, essv15103296, essv15103319
SamplesNA19028, HG02583, NA19664, NA19399, HG03111, HG01079, HG03057, HG03300, HG03241, HG02852, HG02419, HG02891, HG02804, HG03298, NA20298, NA18504, HG02589, NA19374, HG03464, NA19201, HG02952, HG02485, HG02541, NA18916, HG03342, HG02111, NA19922, HG03460, HG02561, HG03189, NA18874, NA19137, HG03045, HG02946, HG01048, HG02882, HG02716, HG02570, NA19908, NA18934, NA19175, HG03291, HG02144, HG02307, NA20126, HG03081, HG03124, HG01049, HG02577, HG01497, HG03046, NA19095, HG02586, HG02282, HG02667, NA19473, HG02983, NA19331, HG02837, NA19334, HG03433, HG02274, NA19467, HG00256, HG03419, HG03103, HG03565, NA19438, HG03313, HG03049, HG02768, HG02676, HG02861, HG03118, HG03439, NA19153, HG03271
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635393
Frequency
Sample Size2504
Observed Gain0
Observed Loss77
Observed Complex0
Frequencyn/a


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