A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621139



Internal ID6661319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94742980..94750635hg38UCSC Ensembl
chr9:97505262..97512917hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg387656
hg197656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13571500
SamplesHG03130
Known GenesC9orf3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621139
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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