A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3551336



Internal ID18849617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32471634..33810426hg38UCSC Ensembl
Innerchr16:32482955..33612893hg19UCSC Ensembl
Innerchr16:32390456..33520394hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381338793
hg191129939
hg181129939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056731
Supporting Variants
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)nssv3551336
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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