A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622295



Internal ID7009154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8857656..8870060hg38UCSC Ensembl
chr10:8899619..8912023hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3812405
hg1912405
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13690409
SamplesHG04056
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622295
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