A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657935



Internal ID9924040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61496171..61501750hg38UCSC Ensembl
Outerchr11:61496134..61501800hg38UCSC Ensembl
Innerchr11:61263643..61269222hg19UCSC Ensembl
Outerchr11:61263606..61269272hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg385667
hg195667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6224523, essv5702073, essv6315107
SamplesNA19000, NA18953, NA18983
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657935
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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