A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675795



Internal ID9941900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:26372197..26376917hg38UCSC Ensembl
Outerchr16:26372160..26376967hg38UCSC Ensembl
Innerchr16:26383518..26388238hg19UCSC Ensembl
Outerchr16:26383481..26388288hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg384808
hg194808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6592748, essv6475034
SamplesNA18599, NA18610
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675795
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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