A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3551294



Internal ID18849575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32447067..33829351hg38UCSC Ensembl
Innerchr16:32458388..33631818hg19UCSC Ensembl
Innerchr16:32365889..33539319hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381382285
hg191173431
hg181173431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063452
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)nssv3551294
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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