A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573522



Internal ID16360931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86154021..86164646hg38UCSC Ensembl
Innerchr16:86187627..86198252hg19UCSC Ensembl
Innerchr16:84745128..84755753hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3810626
hg1910626
hg1810626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv862311
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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