A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062005



Internal ID18804536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32269023..33810426hg38UCSC Ensembl
Innerchr16:32280344..33612893hg19UCSC Ensembl
Innerchr16:32187845..33520394hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381541404
hg191332550
hg181332550
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2839n100
Supporting Variantsnssv3550562
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)nsv1062005
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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