A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573288



Internal ID16360697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79458366..79486656hg38UCSC Ensembl
Innerchr16:79492263..79520553hg19UCSC Ensembl
Innerchr16:78049764..78078054hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3828291
hg1928291
hg1828291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv861694
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573288
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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