A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573520



Internal ID16360929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86080055..86085851hg38UCSC Ensembl
Innerchr16:86113661..86119457hg19UCSC Ensembl
Innerchr16:84671162..84676958hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg385797
hg195797
hg185797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv862309
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573520
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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