A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063528



Internal ID19152747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32447067..33908301hg38UCSC Ensembl
Innerchr16:32458388..33710768hg19UCSC Ensembl
Innerchr16:32365889..33618269hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381461235
hg191252381
hg181252381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2873n100
Supporting Variantsnssv3717162, nssv3551296, nssv3717163, nssv3551295
Samples
Known GenesLOC390705, RNU6-76P, 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)nsv1063528
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer