A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547112



Internal ID18498707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20327288..20411678hg38UCSC Ensembl
Innerchr16:20338610..20423000hg19UCSC Ensembl
Innerchr16:20246111..20330501hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3884391
hg1984391
hg1884391
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052975
Supporting Variants
Samples
Known GenesACSM5, GP2, PDILT, UMOD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3547112
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