A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665016



Internal ID9931121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:34788834..34795070hg38UCSC Ensembl
Outerchr17:34788797..34795120hg38UCSC Ensembl
Innerchr17:33115853..33122089hg19UCSC Ensembl
Outerchr17:33115816..33122139hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386324
hg196324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5780581, essv5411291
SamplesNA20507, NA19720
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665016
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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