A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3558376



Internal ID18856657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35236333..35484929hg38UCSC Ensembl
Innerchr16:34470704..34719300hg19UCSC Ensembl
Innerchr16:34328205..34576801hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38248597
hg19248597
hg18248597
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058753
Supporting Variants
Samples
Known GenesLOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3558376
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