A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666328



Internal ID9585747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109680594..109703400hg38UCSC Ensembl
Outerchr1:109680223..109703770hg38UCSC Ensembl
Innerchr1:110223216..110246022hg19UCSC Ensembl
Outerchr1:110222845..110246392hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3823548
hg1923548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv61e199
Supporting Variantsessv5987471, essv6297268, essv5447782, essv5883274, essv5931609, essv6565567, essv6555276, essv5965682, essv5691566, essv6021170, essv6021030, essv6583889, essv6354191, essv5943864, essv5744185, essv6231679, essv5950400, essv5962316, essv5865155, essv6114729, essv5509502, essv5600578, essv5675181, essv5701424, essv6281460, essv6259093, essv5541480, essv6470673, essv5475348, essv6587331, essv6444672, essv5873617, essv6349232, essv5413788, essv6050548, essv6060883, essv6190410, essv5705405, essv6467871, essv5638396, essv5421844, essv5746961, essv5618677, essv5843969, essv5523437, essv5980575, essv5896756, essv6165281, essv5571770, essv5676807, essv6171722, essv6282236, essv5753035, essv5561777, essv5813030, essv6175494, essv6595630, essv5561575, essv6271747, essv6314167, essv5937268, essv5666191, essv5439115, essv5512129, essv5780513, essv6420293, essv6108039, essv5606438, essv5585798, essv5891776, essv6027274, essv5973837, essv5791019, essv5731617, essv6049446, essv5566827
SamplesNA20588, NA20529, NA20543, NA20766, NA20508, NA20783, NA20514, NA20531, NA20816, NA20813, NA20752, NA20802, NA20532, NA20512, NA20805, NA20808, NA20517, NA20507, NA20771, NA20806, NA20814, NA20586, NA20774, NA20795, NA20769, NA20768, NA20540, NA20513, NA20541, NA20759, NA20539, NA20518, NA20775, NA20533, NA20515, NA20753, NA20818, NA20535, NA20524, NA20505, NA20809, NA20810, NA20760, NA20536, NA20506, NA20519, NA20770, NA20525, NA20538, NA20828, NA20542, NA20534, NA20522, NA20801, NA20804, NA20520, NA20785, NA20790, NA20530, NA20527, NA20778, NA20504, NA20544, NA20516, NA20797, NA20582, NA20510, NA20807, NA20758, NA20826, NA20528, NA20502, NA20585, NA20754, NA20772, NA20509
Known GenesGSTM1, GSTM2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666328
Frequency
Sample Size1151
Observed Gain0
Observed Loss76
Observed Complex0
Frequencyn/a


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