A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3590768



Internal ID6978096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:51630374..51640477hg38UCSC Ensembl
Innerchr2:51630387..51640465hg38UCSC Ensembl
Outerchr2:51630362..51640490hg38UCSC Ensembl
chr2:51857512..51867615hg19UCSC Ensembl
Innerchr2:51857525..51867603hg19UCSC Ensembl
Outerchr2:51857500..51867628hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3810104
hg1910104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10503634
SamplesHG03888
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3590768
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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