A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3704867



Internal ID19003148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:191664863..191975723hg38UCSC Ensembl
Innerchr1:191633993..191944853hg19UCSC Ensembl
Innerchr1:189900616..190211476hg18UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38310861
hg19310861
hg18310861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999147
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)nssv3704867
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