A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526461



Internal ID15453754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31959693..31980322hg38UCSC Ensembl
Innerchr13:32533830..32554459hg19UCSC Ensembl
Innerchr13:31431830..31452459hg18UCSC Ensembl
Innerchr13:31431830..31452459hg17UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3820630
hg1920630
hg1820630
hg1720630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702764
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526461
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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