A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11359738



Internal ID3461440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14419185..14475730hg38UCSC Ensembl
chr4:14420809..14477354hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3856546
hg1956546
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599722
Supporting Variants
SamplesHG03082
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11359738
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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