A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625918



Internal ID7012752
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14090132
SamplesNA19207
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625918
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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