A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573279



Internal ID16360688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78877204..78948438hg38UCSC Ensembl
Innerchr16:78911101..78982335hg19UCSC Ensembl
Innerchr16:77468602..77539836hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3871235
hg1971235
hg1871235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149298
Samples1780854295_A
Known GenesWWOX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573279
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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