A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059532



Internal ID19148751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81947954..81961572hg38UCSC Ensembl
Innerchr16:81981559..81995177hg19UCSC Ensembl
Innerchr16:80539060..80552678hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3813619
hg1913619
hg1813619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559841
Samples
Known GenesPLCG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059532
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