A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667416



Internal ID9586835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:22840615..22844958hg38UCSC Ensembl
Outerchr16:22840458..22845111hg38UCSC Ensembl
Innerchr16:22851936..22856279hg19UCSC Ensembl
Outerchr16:22851779..22856432hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg384654
hg194654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5817900
SamplesNA19472
Known GenesHS3ST2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667416
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer