A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655702



Internal ID15045668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33134619..33283163hg38UCSC Ensembl
Innerchr9:33134617..33283161hg19UCSC Ensembl
Innerchr9:33124617..33273161hg18UCSC Ensembl
Innerchr9:33124617..33273161hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38148545
hg19148545
hg18148545
hg17148545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519369
Supporting Variants
Samples
Known GenesB4GALT1, BAG1, CHMP5, LOC101929639, SPINK4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655702
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