A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3550561



Internal ID18502156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32269023..33735125hg38UCSC Ensembl
Innerchr16:32280344..33537592hg19UCSC Ensembl
Innerchr16:32187845..33445093hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381466103
hg191257249
hg181257249
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058856
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)nssv3550561
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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