A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636698



Internal ID7023492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62307996..62321068hg38UCSC Ensembl
chr15:62600195..62613267hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3813073
hg1913073
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15266031, essv15266032
SamplesHG00599, NA18542
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636698
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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