A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663647



Internal ID9929752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31238491..31250510hg38UCSC Ensembl
Outerchr16:31238454..31250560hg38UCSC Ensembl
Innerchr16:31249812..31261831hg19UCSC Ensembl
Outerchr16:31249775..31261881hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3812107
hg1912107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6498191
SamplesNA18623
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663647
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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