A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688882



Internal ID18640477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34336344..34408206hg38UCSC Ensembl
Innerchr9:34336342..34408204hg19UCSC Ensembl
Innerchr9:34326342..34398204hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3871863
hg1971863
hg1871863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016251
Supporting Variants
Samples
Known GenesC9orf24, FAM219A, KIAA1161, NUDT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3688882
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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