A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14071735



Internal ID5233174
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625766
Supporting Variants
SamplesNA18627
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14071735
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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