A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3550579



Internal ID18848860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32269023..33970586hg38UCSC Ensembl
Innerchr16:32280344..33773053hg19UCSC Ensembl
Innerchr16:32187845..33680554hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381701564
hg191492710
hg181492710
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061743
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)nssv3550579
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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