A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661585



Internal ID9927690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:67815651..67817284hg38UCSC Ensembl
Outerchr16:67815614..67817334hg38UCSC Ensembl
Innerchr16:67849554..67851187hg19UCSC Ensembl
Outerchr16:67849517..67851237hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381721
hg191721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv502e199
Supporting Variantsessv6145401, essv5403762
SamplesNA18873, NA19116
Known GenesTSNAXIP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661585
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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