A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518977



Internal ID15099584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33675631..33845081hg38UCSC Ensembl
Innerchr9:33675629..33845079hg19UCSC Ensembl
Innerchr9:33665629..33835079hg18UCSC Ensembl
Innerchr9:33665629..33835079hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38169451
hg19169451
hg18169451
hg17169451
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696445
Samples
Known GenesLOC101929688, PRSS3, PTENP1, PTENP1-AS, UBE2R2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518977
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