A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573422



Internal ID16014145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84178502..84180359hg38UCSC Ensembl
Innerchr16:84212108..84213965hg19UCSC Ensembl
Innerchr16:82769609..82771466hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381858
hg191858
hg181858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv862001
Samples
Known GenesTAF1C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573422
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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