A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15198901



Internal ID2695713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28232706..28294113hg38UCSC Ensembl
chr15:28477852..28539259hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3861408
hg1961408
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635992
Supporting Variants
SamplesHG02384
Known GenesHERC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15198901
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