A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065333



Internal ID18807864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:52543923..52582078hg38UCSC Ensembl
Innerchr16:52577835..52615990hg19UCSC Ensembl
Innerchr16:51135336..51173491hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3838156
hg1938156
hg1838156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559261
Samples
Known GenesCASC16, TOX3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065333
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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