A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522900



Internal ID15103507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3377101..3378408hg38UCSC Ensembl
Innerchr1:3293665..3294972hg19UCSC Ensembl
Innerchr1:3283525..3284832hg18UCSC Ensembl
Innerchr1:3316822..3318129hg17UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg381308
hg191308
hg181308
hg171308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698558
Samples
Known GenesPRDM16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522900
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