A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662033



Internal ID9581452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67670068..67670248hg38UCSC Ensembl
Outerchr11:67670031..67670298hg38UCSC Ensembl
Innerchr11:67437539..67437719hg19UCSC Ensembl
Outerchr11:67437502..67437769hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6546317, essv5661487, essv6562487, essv5568981, essv5641051, essv5783003, essv6289208, essv6390238, essv6024884, essv6382539, essv6370973, essv5924155, essv5598112, essv6444027, essv6464789, essv6015673, essv6406399, essv5903266, essv5985870, essv5705306, essv6202726, essv6017826, essv5881632, essv6402771, essv6315444, essv6179325, essv6555270, essv5729127, essv5942428, essv6402953, essv5567911, essv5835735, essv5700283, essv6012099, essv5824773, essv5944686, essv5869834, essv5799063, essv6306726, essv6366940, essv6352906, essv6543971, essv6529885, essv5988563, essv5599239, essv6591829, essv5678062, essv5791249, essv5885235, essv6565699, essv5894393, essv6412053, essv6582384, essv5472780, essv5513318, essv5708353, essv6509573, essv5618416, essv5727593, essv5704197, essv5714100, essv6088448, essv6054553, essv6170727, essv5532541, essv6306486
SamplesHG00323, HG00313, HG00537, HG00536, HG01440, HG00257, HG00619, HG01353, NA18530, HG00418, HG00437, HG01173, HG00464, NA19311, HG00707, NA19359, HG01051, HG00375, HG01174, HG00701, HG00683, HG00111, HG00581, HG00651, HG00335, HG01101, HG00319, HG00253, NA18559, HG01375, NA18623, HG00692, HG00689, HG00330, HG00419, HG00125, HG00343, HG00584, HG00620, HG01437, NA18537, HG01066, HG01073, HG00513, HG00524, HG00512, HG01070, NA19382, NA18606, HG00590, HG01095, HG00443, HG01334, HG00650, NA19403, NA18602, NA19818, HG00285, HG00656, HG00422, HG00693, HG00324, HG00137, NA19381, HG00684, HG00704
Known GenesALDH3B2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662033
Frequency
Sample Size1151
Observed Gain0
Observed Loss66
Observed Complex0
Frequencyn/a


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