A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517914



Internal ID15445207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:118396363..119029921hg38UCSC Ensembl
Innerchr9:121158641..121792199hg19UCSC Ensembl
Innerchr9:120198462..120832020hg18UCSC Ensembl
Innerchr9:118238195..118871753hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38633559
hg19633559
hg18633559
hg17633559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695326
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517914
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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