A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065967



Internal ID19155186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32169453..32560003hg38UCSC Ensembl
Innerchr16:32180774..32571324hg19UCSC Ensembl
Innerchr16:32088275..32478825hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38390551
hg19390551
hg18390551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2853n100
Supporting Variantsnssv3550363, nssv3550365, nssv3550364
Samples
Known GenesLOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065967
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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