A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619298



Internal ID7006176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2745732..2816795hg38UCSC Ensembl
chr9:2745732..2816795hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3871064
hg1971064
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13380581, essv13380582
SamplesHG00442, NA19443
Known GenesKIAA0020
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619298
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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