A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv462e59



Internal ID20127211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77470788..77472786hg38UCSC Ensembl
chr10:79230546..79232544hg19UCSC Ensembl
chr10:78900552..78902550hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381999
hg191999
hg181999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3358173, esv3413778
SamplesNA19239, NA19240
Known GenesKCNMA1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv462e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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