A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675677



Internal ID9941782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:16953845..16977406hg38UCSC Ensembl
Outerchr3:16953808..16977456hg38UCSC Ensembl
Innerchr3:16995337..17018898hg19UCSC Ensembl
Outerchr3:16995300..17018948hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3823649
hg1923649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5760069
SamplesHG01465
Known GenesPLCL2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675677
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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