A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3550513



Internal ID18502108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32233140..34026275hg38UCSC Ensembl
Innerchr16:32244461..33828742hg19UCSC Ensembl
Innerchr16:32151962..33736243hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381793136
hg191584282
hg181584282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061494
Supporting Variants
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3550513
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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