A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv859123



Internal ID16153079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:71954829..71986424hg38UCSC Ensembl
Innerchr16:71988728..72020323hg19UCSC Ensembl
Innerchr16:70546229..70577824hg18UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3831596
hg1931596
hg1831596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572950
Supporting Variants
Samples
Known GenesPKD1L3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv859123
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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