A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10943641



Internal ID4213792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20351184..20514664hg38UCSC Ensembl
chr3:20392676..20556156hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38163481
hg19163481
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595478
Supporting Variants
SamplesHG03790
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10943641
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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