A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061564



Internal ID19150783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32526896..33952512hg38UCSC Ensembl
Innerchr16:32538217..33754979hg19UCSC Ensembl
Innerchr16:32445718..33662480hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381425617
hg191216763
hg181216763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2876n100
Supporting Variantsnssv3551851
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)nsv1061564
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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