A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14287952



Internal ID6810276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112824777..112851171hg38UCSC Ensembl
Innerchr11:112824777..112851171hg38UCSC Ensembl
Outerchr11:112824277..112851671hg38UCSC Ensembl
chr11:112695500..112721894hg19UCSC Ensembl
Innerchr11:112695500..112721894hg19UCSC Ensembl
Outerchr11:112695000..112722394hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3826395
hg1926395
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627766
Supporting Variants
SamplesNA20894
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14287952
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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