A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559499



Internal ID18511094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70015881..70118407hg38UCSC Ensembl
Innerchr16:70049784..70152310hg19UCSC Ensembl
Innerchr16:68607285..68709811hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38102527
hg19102527
hg18102527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066093
Supporting Variants
Samples
Known GenesMIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559499
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