A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11359155



Internal ID5178158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13259639..13289412hg38UCSC Ensembl
chr4:13261263..13291036hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3829774
hg1929774
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599699
Supporting Variants
SamplesNA18605
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11359155
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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