A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv862246



Internal ID16156202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85269021..85275515hg38UCSC Ensembl
Innerchr16:85302627..85309121hg19UCSC Ensembl
Innerchr16:83860128..83866622hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg386495
hg196495
hg186495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573483
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)nssv862246
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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