A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559255



Internal ID18510850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:50744296..50793690hg38UCSC Ensembl
Innerchr16:50778207..50827601hg19UCSC Ensembl
Innerchr16:49335708..49385102hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3849395
hg1949395
hg1849395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058852
Supporting Variants
Samples
Known GenesCYLD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559255
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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