A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690938



Internal ID18989219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46587..218183hg38UCSC Ensembl
Innerchr9:46587..218183hg19UCSC Ensembl
Innerchr9:36587..208183hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38171597
hg19171597
hg18171597
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031865
Supporting Variants
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690938
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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