A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3591506



Internal ID6978834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84124677..84133498hg38UCSC Ensembl
Innerchr2:84124827..84133348hg38UCSC Ensembl
Outerchr2:84124527..84133648hg38UCSC Ensembl
chr2:84351801..84360622hg19UCSC Ensembl
Innerchr2:84351951..84360472hg19UCSC Ensembl
Outerchr2:84351651..84360772hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg388822
hg198822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10564679
SamplesNA20882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3591506
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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