A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656812



Internal ID9922917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62794468..62807392hg38UCSC Ensembl
chr16:62828372..62841296hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3812925
hg1912925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6191709
SamplesHG01075
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656812
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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