A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14243295



Internal ID6417056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95150469..95151034hg38UCSC Ensembl
Innerchr11:95150470..95151034hg38UCSC Ensembl
Outerchr11:95150469..95151035hg38UCSC Ensembl
chr11:94883633..94884198hg19UCSC Ensembl
Innerchr11:94883634..94884198hg19UCSC Ensembl
Outerchr11:94883633..94884199hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627338
Supporting Variants
SamplesNA20362
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14243295
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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