A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14232912



Internal ID5503511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91023134..91096097hg38UCSC Ensembl
Innerchr11:91023145..91096087hg38UCSC Ensembl
Outerchr11:91023124..91096108hg38UCSC Ensembl
chr11:90756302..90829265hg19UCSC Ensembl
Innerchr11:90756313..90829255hg19UCSC Ensembl
Outerchr11:90756292..90829276hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3872964
hg1972964
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627232
Supporting Variants
SamplesNA18986
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14232912
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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