A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624554



Internal ID7011407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111235239..111253929hg38UCSC Ensembl
chr10:112994997..113013687hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3818691
hg1918691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13935583
SamplesHG03007
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624554
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer