A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5577995



Internal ID9907100
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 Flag1
Merged StatusS
Merged Variantsesv2668939
Supporting Variants
SamplesNA20802
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5577995
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