A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5604775



Internal ID9367757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83602276..83687908hg38UCSC Ensembl
Outerchr13:83602239..83687958hg38UCSC Ensembl
Innerchr13:84176411..84262043hg19UCSC Ensembl
Outerchr13:84176374..84262093hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3885720
hg1985720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659085
Supporting Variants
SamplesNA18561
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5604775
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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