A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656594



Internal ID2889681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189878673..189878873hg38UCSC Ensembl
chr3:189596462..189596662hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6232532, essv6062574, essv6354909, essv5810162, essv5748213, essv5987880, essv5963252, essv6337545, essv5665501, essv6260317, essv6038801, essv5947412, essv6180871, essv5802111, essv5482302, essv5935151, essv5617132, essv6168055, essv6524467, essv5876158, essv5865380, essv5881844, essv6189650, essv5945351, essv5977973, essv5553524, essv6182700, essv6262603, essv5552438, essv5547030, essv6086449, essv5672910, essv6097610, essv6058088, essv6497322, essv5710077, essv6073213, essv6530713, essv5489360, essv5718943, essv5446654, essv5855320, essv5580992, essv5959793, essv5894214, essv5980066, essv5834302, essv5733322, essv5588755, essv6040488, essv6178975, essv5744321, essv6400394, essv5999182, essv5806098, essv5856233, essv6596810, essv5615455, essv6145269, essv6268158, essv5758614, essv5706616, essv6580915, essv5958625, essv6491013, essv5624514, essv6115674, essv5509168, essv6578685, essv5868324, essv6204107, essv5725866, essv6405699, essv5967138, essv6368323, essv6313591, essv5843076, essv6413585, essv5546067, essv6148452, essv5623233, essv6128107, essv6378798
SamplesHG00313, HG00252, HG00318, NA18595, HG00619, HG01353, HG00418, HG01072, NA19404, HG01055, HG01173, HG00186, HG00131, HG00310, HG00657, HG00614, HG01365, HG00428, HG00475, HG00326, HG00139, HG00701, HG00334, HG01204, HG00280, HG00319, HG01171, NA18632, HG00342, HG01107, NA18559, HG00346, NA18624, NA18536, NA18623, HG01048, HG00692, HG01047, NA18636, HG00315, HG00125, HG00258, NA19663, HG00284, HG01187, HG00343, NA19360, NA19380, NA18620, NA19374, NA19393, HG00260, HG00501, HG00273, HG00282, HG01170, HG00232, HG00249, HG00524, HG00525, HG01060, NA18543, NA19376, NA18599, HG00650, NA19394, HG00530, NA18548, HG00285, HG00656, HG00320, HG00275, NA18549, HG00473, HG00137, HG01102, HG01462, HG00704, HG00271, HG00278, HG01067, HG01354, HG00327
Known GenesTP63
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656594
Frequency
Sample Size1151
Observed Gain0
Observed Loss83
Observed Complex0
Frequencyn/a


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