A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526306



Internal ID15453599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85948640..85950994hg38UCSC Ensembl
Innerchr16:85982246..85984600hg19UCSC Ensembl
Innerchr16:84539747..84542101hg18UCSC Ensembl
Innerchr16:84539747..84542101hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382355
hg192355
hg182355
hg172355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702589
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526306
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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