A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15219615



Internal ID770840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37358658..37440379hg38UCSC Ensembl
chr15:37650859..37732580hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3881722
hg1981722
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636173
Supporting Variants
SamplesHG00365
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15219615
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