A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678178



Internal ID9944283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10798102..10799460hg38UCSC Ensembl
Outerchr16:10798065..10799510hg38UCSC Ensembl
Innerchr16:10891959..10893317hg19UCSC Ensembl
Outerchr16:10891922..10893367hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381446
hg191446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5582201
SamplesNA20518
Known GenesTVP23A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678178
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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