A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3675233



Internal ID18626828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2378491..3295843hg38UCSC Ensembl
Innerchr8:2301535..3153365hg19UCSC Ensembl
Innerchr8:2288942..3140772hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38917353
hg19851831
hg18851831
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015411
Supporting Variants
Samples
Known GenesCSMD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3675233
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