A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688885



Internal ID18640480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35084357..35506646hg38UCSC Ensembl
Innerchr9:35084354..35506643hg19UCSC Ensembl
Innerchr9:35074354..35496643hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38422290
hg19422290
hg18422290
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030303
Supporting Variants
Samples
Known GenesATP8B5P, FAM214B, PIGO, RUSC2, STOML2, UNC13B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3688885
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