A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525887



Internal ID15453180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18778321..18791357hg38UCSC Ensembl
Innerchr9:18778319..18791355hg19UCSC Ensembl
Innerchr9:18768319..18781355hg18UCSC Ensembl
Innerchr9:18768319..18781355hg17UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3813037
hg1913037
hg1813037
hg1713037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702089
Samples
Known GenesADAMTSL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525887
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