A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852344



Internal ID16146300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5432142..5569788hg38UCSC Ensembl
Innerchr16:5482143..5619789hg19UCSC Ensembl
Innerchr16:5422144..5559790hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38137647
hg19137647
hg18137647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571306
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)nssv852344
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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