A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642665



Internal ID7029434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59616809..59618811hg38UCSC Ensembl
Innerchr18:59616823..59618798hg38UCSC Ensembl
Outerchr18:59616796..59618825hg38UCSC Ensembl
chr18:57284041..57286043hg19UCSC Ensembl
Innerchr18:57284055..57286030hg19UCSC Ensembl
Outerchr18:57284028..57286057hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg382003
hg192003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15895646
SamplesHG02013
Known GenesCCBE1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642665
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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