A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718836



Internal ID18670431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5122225..5298137hg38UCSC Ensembl
Innerchr16:5172226..5348138hg19UCSC Ensembl
Innerchr16:5112227..5288139hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38175913
hg19175913
hg18175913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045686
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718836
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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