A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616677



Internal ID6656873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25210519..25221990hg38UCSC Ensembl
Innerchr8:25211019..25221490hg38UCSC Ensembl
Outerchr8:25209519..25222990hg38UCSC Ensembl
chr8:25068035..25079506hg19UCSC Ensembl
Innerchr8:25068535..25079006hg19UCSC Ensembl
Outerchr8:25067035..25080506hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3811472
hg1911472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13142712
SamplesNA19213
Known GenesDOCK5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616677
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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