A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559673



Internal ID18511268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77894052..78561070hg38UCSC Ensembl
Innerchr16:77927949..78594967hg19UCSC Ensembl
Innerchr16:76485450..77152468hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38667019
hg19667019
hg18667019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055930
Supporting Variants
Samples
Known GenesCLEC3A, VAT1L, WWOX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559673
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