A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5702073



Internal ID9503318
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 Flag1
Merged StatusS
Merged Variantsesv2657935
Supporting Variants
SamplesNA18983
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5702073
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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