A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669224



Internal ID9935329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63373287..63391624hg38UCSC Ensembl
Outerchr20:63373246..63391688hg38UCSC Ensembl
Innerchr20:62004639..62022977hg19UCSC Ensembl
Outerchr20:62004598..62023041hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3818443
hg1918444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5624049
SamplesHG01462
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669224
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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