A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662850



Internal ID9582269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65842768..65843041hg38UCSC Ensembl
chr11:65610239..65610512hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6060468, essv6384615, essv6526726, essv5691640, essv5397104, essv5859453, essv6294468, essv5926740, essv6199116, essv5865659, essv6385293, essv5656596, essv5431231, essv5966949, essv5947876, essv5770818, essv5775550, essv6045978, essv5702613, essv5413724, essv6590699, essv5584638, essv5548420, essv5984642
SamplesHG00607, NA18595, NA18612, HG00464, HG00707, NA18948, HG00428, HG00698, NA18557, HG00556, NA18624, HG00583, NA18536, NA18623, NA18638, HG00653, HG00513, HG00534, NA18552, NA18565, NA18560, HG00654, HG00476, HG00531
Known GenesSNX32
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662850
Frequency
Sample Size1151
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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