A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625766



Internal ID7012600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27232343..27233519hg38UCSC Ensembl
Innerchr11:27232343..27233519hg38UCSC Ensembl
Outerchr11:27232142..27233668hg38UCSC Ensembl
chr11:27253890..27255066hg19UCSC Ensembl
Innerchr11:27253890..27255066hg19UCSC Ensembl
Outerchr11:27253689..27255215hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381177
hg191177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14071735, essv14071734
SamplesNA18627, HG00708
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625766
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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