A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10979524



Internal ID5509667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34439621..34589742hg38UCSC Ensembl
chr3:34481113..34631234hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38150122
hg19150122
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595814
Supporting Variants
SamplesNA18988
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10979524
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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