A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3551137



Internal ID18849418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32369618..34060384hg38UCSC Ensembl
Innerchr16:32380939..33862851hg19UCSC Ensembl
Innerchr16:32288440..33770352hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381690767
hg191481913
hg181481913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057228
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)nssv3551137
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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