A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893479



Internal ID19184299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36398139..36453868hg38UCSC Ensembl
Outerchr22:36398139..36453868hg38UCSC Ensembl
Innerchr22:36794184..36849915hg19UCSC Ensembl
Outerchr22:36794184..36849915hg19UCSC Ensembl
Innerchr22:35124130..35179861hg18UCSC Ensembl
Outerchr22:35124130..35179861hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3855730
hg1955732
hg1855732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787350
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893479
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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