A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3493801



Internal ID18734756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:159992675..160020138hg38UCSC Ensembl
Innerchr1:159962465..159989928hg19UCSC Ensembl
Innerchr1:158229089..158256552hg18UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3827464
hg1927464
hg1827464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007787
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3493801
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