A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624674



Internal ID6664837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117141857..117425204hg38UCSC Ensembl
chr10:118901368..119184715hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38283348
hg19283348
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13946455
SamplesHG02983
Known GenesKCNK18, MIR3663, PDZD8, SLC18A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624674
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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