A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065281



Internal ID19154500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79307678..79330945hg38UCSC Ensembl
Innerchr16:79341575..79364842hg19UCSC Ensembl
Innerchr16:77899076..77922343hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3823268
hg1923268
hg1823268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559771
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065281
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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