A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636312



Internal ID7023108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44817078..44825278hg38UCSC Ensembl
chr15:45109276..45117476hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg388201
hg198201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15233280
SamplesHG01345
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636312
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