A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3550369



Internal ID18848650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32169453..32644190hg38UCSC Ensembl
Innerchr16:32180774..32655511hg19UCSC Ensembl
Innerchr16:32088275..32563012hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38474738
hg19474738
hg18474738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062262
Supporting Variants
Samples
Known GenesLOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3550369
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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