A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716944



Internal ID19015225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19932666..19956028hg38UCSC Ensembl
Innerchr16:19943988..19967350hg19UCSC Ensembl
Innerchr16:19851489..19874851hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3823363
hg1923363
hg1823363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046555
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)nssv3716944
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer