A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5607270



Internal ID8584673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69639548..69643554hg38UCSC Ensembl
Outerchr11:69639177..69643924hg38UCSC Ensembl
Innerchr11:69454316..69458322hg19UCSC Ensembl
Outerchr11:69453945..69458692hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg384748
hg194748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675336
Supporting Variants
SamplesNA19062
Known GenesCCND1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5607270
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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