A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066152



Internal ID19155371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32618616..33818870hg38UCSC Ensembl
Innerchr16:32629937..33621337hg19UCSC Ensembl
Innerchr16:32537438..33528838hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381200255
hg19991401
hg18991401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2876n100
Supporting Variantsnssv3551975
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)nsv1066152
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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