A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14890288



Internal ID3521238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106299348..106337573hg38UCSC Ensembl
chr13:106951697..106989921hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3838226
hg1938225
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633461
Supporting Variants
SamplesHG03118
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14890288
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