A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528884



Internal ID15109491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:116036395..116103136hg38UCSC Ensembl
Innerchr1:116579016..116645757hg19UCSC Ensembl
Innerchr1:116380539..116447280hg18UCSC Ensembl
Innerchr1:116291058..116357799hg17UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg3866742
hg1966742
hg1866742
hg1766742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705565
Samples
Known GenesSLC22A15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528884
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