A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11265052



Internal ID3126108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188999209..189014402hg38UCSC Ensembl
chr3:188716998..188732191hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3815194
hg1915194
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599045
Supporting Variants
SamplesHG02757
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11265052
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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