A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059367



Internal ID18801898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:47490795..47552424hg38UCSC Ensembl
Innerchr16:47524706..47586335hg19UCSC Ensembl
Innerchr16:46082207..46143836hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3861630
hg1961630
hg1861630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722702
Samples
Known GenesPHKB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059367
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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