A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621121



Internal ID7007990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94425084..94482251hg38UCSC Ensembl
chr9:97187366..97244533hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3857168
hg1957168
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13569801
SamplesHG04229
Known GenesHIATL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621121
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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