A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676295



Internal ID9942400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64649067..64651303hg38UCSC Ensembl
chr16:64682970..64685206hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382237
hg192237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5987333, essv6172917
SamplesHG00343, HG00377
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676295
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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