A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067006



Internal ID18809537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:50747807..50798809hg38UCSC Ensembl
Innerchr16:50781718..50832720hg19UCSC Ensembl
Innerchr16:49339219..49390221hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3851003
hg1951003
hg1851003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2977n100
Supporting Variantsnssv3559256
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)nsv1067006
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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