A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669633



Internal ID9935738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184962353..184962434hg38UCSC Ensembl
chr4:185883507..185883588hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5715788, essv5707387, essv6211500, essv6001913, essv6260979, essv6088922, essv6428888, essv5991518, essv5730920, essv6369626, essv5919170, essv6480937, essv6006927, essv5648340, essv6219462, essv6235593, essv6214053, essv5617306, essv5574271, essv5712445, essv5826930, essv6477652, essv6396937, essv6150732, essv5721265, essv5979698, essv5413620, essv6457508, essv6013889, essv5744613, essv6149143, essv6492887, essv5531574, essv6222872, essv6085938, essv5485511, essv6262876, essv5859222, essv6232841, essv5905974, essv5948500, essv5768998, essv6494162, essv6198544, essv5769804, essv6027757, essv5476452, essv5826459, essv5982417, essv6512509, essv6204184, essv6113511, essv5398136, essv5988597, essv6356719, essv5572148, essv5917847, essv5606187, essv6145037, essv6556823, essv5424072, essv5957809, essv6144325, essv5897814, essv6279533, essv6483782, essv5965510, essv6016975, essv5949036, essv5826307, essv6355531, essv6333478, essv6461272, essv6132078, essv6173156, essv6267097, essv5635921, essv5943329, essv5742533, essv6514926, essv6254847, essv5810422, essv5674168, essv6187225, essv5848619, essv5582165, essv6159204, essv5607690, essv6470072, essv5535301, essv5853658, essv5592236, essv5481166, essv5628586, essv5929528, essv6359825, essv5528142, essv5412342, essv5689179
SamplesHG01060, HG01441, HG00650, HG00249, NA11829, HG01052, HG01188, HG00315, NA18603, NA12751, NA18530, NA18606, HG00261, HG00693, HG00327, NA19373, NA18550, HG01351, HG00702, HG00330, NA18571, HG00247, NA19138, HG01365, NA18611, HG00512, HG00139, HG00277, HG01069, HG00335, HG00427, NA18557, HG00323, HG00530, HG00419, HG00253, HG00260, HG01353, HG00543, HG00313, HG00137, HG00154, HG00653, HG00657, HG00475, HG00320, HG00584, HG00533, HG00263, HG00275, HG00692, HG00324, HG00284, HG00273, NA11919, HG00479, NA18532, HG00525, HG00140, HG01334, HG00276, HG00246, HG01107, NA18576, NA18632, NA12716, HG00254, HG00336, HG00285, NA18543, NA18559, HG00375, HG01357, HG01174, HG00319, HG01108, NA19360, NA07037, HG00256, HG00662, HG00418, HG00620, HG00339, HG00125, HG00111, HG00513, HG00421, NA18636, HG00310, HG00186, HG00280, HG00252, HG01378, HG01082, NA18622, HG00437, NA18562, NA18577, NA18620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669633
Frequency
Sample Size1151
Observed Gain0
Observed Loss99
Observed Complex0
Frequencyn/a


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