A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696539



Internal ID15433191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135257320..135344459hg38UCSC Ensembl
Innerchr9:138149166..138236305hg19UCSC Ensembl
Innerchr9:137288987..137376126hg18UCSC Ensembl
Innerchr9:135375111..135462250hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3887140
hg1987140
hg1887140
hg1787140
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517428
Supporting Variants
Samples
Known GenesC9orf62
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696539
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