A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11393902



Internal ID5932198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35253199..35270837hg38UCSC Ensembl
chr4:35254821..35272459hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3817639
hg1917639
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600192
Supporting Variants
SamplesNA19346
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11393902
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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