A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066652



Internal ID19155871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32135553..32804488hg38UCSC Ensembl
Innerchr16:32146874..32815809hg19UCSC Ensembl
Innerchr16:32054375..32723310hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38668936
hg19668936
hg18668936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2841n100
Supporting Variantsnssv3550292
Samples
Known GenesHERC2P4, LOC390705, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066652
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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