A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3550549



Internal ID18848830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32269023..32904180hg38UCSC Ensembl
Innerchr16:32280344..32915501hg19UCSC Ensembl
Innerchr16:32187845..32823002hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38635158
hg19635158
hg18635158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057587
Supporting Variants
Samples
Known GenesLOC390705, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3550549
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