A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11093489



Internal ID3937179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106180012..106189116hg38UCSC Ensembl
chr3:105898859..105907963hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg389105
hg199105
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597283
Supporting Variants
SamplesHG03593
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11093489
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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