A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14084226



Internal ID3961604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32451027..32458111hg38UCSC Ensembl
Innerchr11:32451027..32458111hg38UCSC Ensembl
Outerchr11:32450527..32458611hg38UCSC Ensembl
chr11:32472573..32479657hg19UCSC Ensembl
Innerchr11:32472573..32479657hg19UCSC Ensembl
Outerchr11:32472073..32480157hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg387085
hg197085
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625863
Supporting Variants
SamplesHG03615
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14084226
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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