A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658544



Internal ID9924649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76431283..76437507hg38UCSC Ensembl
chr11:76142327..76148551hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg386225
hg196225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6472769, essv6223922, essv6002953, essv6545582, essv6443135, essv5568679, essv6429882, essv5519993, essv6334906, essv6388983, essv5583541, essv6535071, essv6549032, essv6441036, essv6471834, essv6520019, essv5682542, essv6381019, essv6358687, essv6183088, essv5755850, essv6531602, essv6410234, essv6166452, essv5411145
SamplesNA18508, NA19920, NA19107, HG00641, NA19916, NA19904, NA19383, NA19238, NA19385, NA19172, NA19471, NA19200, NA19437, NA18516, NA18907, NA19099, NA19712, HG00638, NA19428, NA19818, NA18501, NA19438, NA19102, NA19316, NA18522
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658544
Frequency
Sample Size1151
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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