A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559342



Internal ID18857623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:56160368..56188613hg38UCSC Ensembl
Innerchr16:56194280..56222525hg19UCSC Ensembl
Innerchr16:54751781..54780026hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3828246
hg1928246
hg1828246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067178
Supporting Variants
Samples
Known GenesLOC283856
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559342
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