A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524467



Internal ID15105074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3391470..3391934hg38UCSC Ensembl
Innerchr1:3308034..3308498hg19UCSC Ensembl
Innerchr1:3297894..3298358hg18UCSC Ensembl
Innerchr1:3331191..3331655hg17UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38465
hg19465
hg18465
hg17465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700403
Samples
Known GenesPRDM16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524467
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