A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852337



Internal ID15799607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4317729..4337423hg38UCSC Ensembl
Innerchr16:4367730..4387424hg19UCSC Ensembl
Innerchr16:4307731..4327425hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3819695
hg1919695
hg1819695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571300
Supporting Variants
Samples
Known GenesGLIS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852337
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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