A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11739566



Internal ID2804922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185472129..185501859hg38UCSC Ensembl
chr4:186393283..186423013hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3829731
hg1929731
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603500
Supporting Variants
SamplesHG02477
Known GenesPDLIM3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11739566
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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