A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14095224



Internal ID987742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38719046..38807308hg38UCSC Ensembl
Innerchr11:38719079..38807275hg38UCSC Ensembl
Outerchr11:38719013..38807341hg38UCSC Ensembl
chr11:38740596..38828858hg19UCSC Ensembl
Innerchr11:38740629..38828825hg19UCSC Ensembl
Outerchr11:38740563..38828891hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3888263
hg1988263
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626016
Supporting Variants
SamplesHG00614
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14095224
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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