A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505994



Internal ID18804275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95319876..95344866hg38UCSC Ensembl
Innerchr11:95053040..95078030hg19UCSC Ensembl
Innerchr11:94692688..94717678hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3824991
hg1924991
hg1824991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039506
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)nssv3505994
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