A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633450



Internal ID7020259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105698543..105703986hg38UCSC Ensembl
Innerchr13:105698543..105703986hg38UCSC Ensembl
Outerchr13:105698332..105704179hg38UCSC Ensembl
chr13:106350892..106356335hg19UCSC Ensembl
Innerchr13:106350892..106356335hg19UCSC Ensembl
Outerchr13:106350681..106356528hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg385444
hg195444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14888908
SamplesNA18570
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633450
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