A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520802



Internal ID15448095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130144207..130226430hg38UCSC Ensembl
Innerchr9:132906486..132988709hg19UCSC Ensembl
Innerchr9:131946307..132028530hg18UCSC Ensembl
Innerchr9:129986040..130068263hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3882224
hg1982224
hg1882224
hg1782224
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681603, nssv694090, nssv701729, nssv675617
Samples
Known GenesNCS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520802
Frequency
Sample Size2026
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer