A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11200142



Internal ID4270792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:162096635..162128520hg38UCSC Ensembl
chr3:161814423..161846308hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3831886
hg1931886
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598427
Supporting Variants
SamplesHG03836
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11200142
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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