A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661671



Internal ID9927776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76961782..76966776hg38UCSC Ensembl
chr11:76672826..76677820hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg384995
hg194995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5890653, essv5939501, essv5552707, essv5672945, essv6278270, essv6097493, essv6394799
SamplesNA19700, NA19704, NA18874, NA19921, NA19982, NA18910, HG01390
Known GenesACER3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661671
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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