A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14090415



Internal ID3620932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35560286..35566211hg38UCSC Ensembl
Innerchr11:35560318..35566180hg38UCSC Ensembl
Outerchr11:35560255..35566243hg38UCSC Ensembl
chr11:35581834..35587759hg19UCSC Ensembl
Innerchr11:35581866..35587728hg19UCSC Ensembl
Outerchr11:35581803..35587791hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385926
hg195926
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625934
Supporting Variants
SamplesHG03212
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14090415
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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