A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668939



Internal ID9935044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67075354..67077444hg38UCSC Ensembl
Outerchr11:67075317..67077494hg38UCSC Ensembl
Innerchr11:66842825..66844915hg19UCSC Ensembl
Outerchr11:66842788..66844965hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg382178
hg192178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5577995, essv6404968, essv5513750
SamplesNA20802, NA12751, HG00330
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668939
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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