A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056972



Internal ID18799503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32269023..34110563hg38UCSC Ensembl
Innerchr16:32280344..33913030hg19UCSC Ensembl
Innerchr16:32187845..33820531hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381841541
hg191632687
hg181632687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2840n100
Supporting Variantsnssv3550592
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)nsv1056972
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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