A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv862957



Internal ID16156913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88547158..88552881hg38UCSC Ensembl
Innerchr16:88613566..88619289hg19UCSC Ensembl
Innerchr16:87141067..87146790hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg385724
hg195724
hg185724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573648
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv862957
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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