A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623188



Internal ID7010045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46001576..46021276hg38UCSC Ensembl
chr10:51574546..51594246hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3819701
hg1919701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13799914, essv13799915
SamplesNA18530, NA18868
Known GenesNCOA4, TIMM23
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623188
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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