A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625899



Internal ID7012733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33905591..33908835hg38UCSC Ensembl
Innerchr11:33905596..33908830hg38UCSC Ensembl
Outerchr11:33905586..33908840hg38UCSC Ensembl
chr11:33927138..33930382hg19UCSC Ensembl
Innerchr11:33927143..33930377hg19UCSC Ensembl
Outerchr11:33927133..33930387hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383245
hg193245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14088546
SamplesNA19031
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625899
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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