A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14090132



Internal ID5833273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35067953..35082987hg38UCSC Ensembl
Innerchr11:35067953..35082987hg38UCSC Ensembl
Outerchr11:35067453..35083487hg38UCSC Ensembl
chr11:35089500..35104534hg19UCSC Ensembl
Innerchr11:35089500..35104534hg19UCSC Ensembl
Outerchr11:35089000..35105034hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3815035
hg1915035
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625918
Supporting Variants
SamplesNA19207
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14090132
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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