A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11463397



Internal ID5488568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64281976..64296684hg38UCSC Ensembl
chr4:65147694..65162402hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3814709
hg1914709
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600761
Supporting Variants
SamplesNA18980
Known GenesTECRL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11463397
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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