A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669755



Internal ID9935860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36781365..36789437hg38UCSC Ensembl
Outerchr17:36781208..36789590hg38UCSC Ensembl
Innerchr17:35138543..35146711hg19UCSC Ensembl
Outerchr17:35138386..35146864hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg388383
hg198479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5640347, essv5903389
SamplesHG01079, NA19474
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669755
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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