A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573286



Internal ID16360695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79137240..79181188hg38UCSC Ensembl
Innerchr16:79171137..79215085hg19UCSC Ensembl
Innerchr16:77728638..77772586hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3843949
hg1943949
hg1843949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv861692
Samples
Known GenesWWOX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573286
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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