A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15235999



Internal ID4112488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45764244..45864872hg38UCSC Ensembl
chr15:46056442..46157070hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38100629
hg19100629
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636346
Supporting Variants
SamplesHG03733
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15235999
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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