A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056366



Internal ID19145585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32016645..32292156hg38UCSC Ensembl
Innerchr16:32027966..32303477hg19UCSC Ensembl
Innerchr16:31935467..32210978hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38275512
hg19275512
hg18275512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2843n100
Supporting Variantsnssv3716193
Samples
Known GenesHERC2P4, LOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056366
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