A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13459066



Internal ID3460882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35058196..35071684hg38UCSC Ensembl
chr9:35058193..35071681hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3813489
hg1913489
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620367
Supporting Variants
SamplesHG02095
Known GenesVCP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13459066
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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