A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11476620



Internal ID3088536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67373806..67419799hg38UCSC Ensembl
chr4:68239524..68285517hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3845994
hg1945994
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600848
Supporting Variants
SamplesHG02715
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11476620
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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