A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573303



Internal ID16360712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80917409..80955962hg38UCSC Ensembl
Innerchr16:80951306..80989859hg19UCSC Ensembl
Innerchr16:79508807..79547360hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3838554
hg1938554
hg1838554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5239n54
Supporting Variantsnssv861706
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573303
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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