A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3548051



Internal ID18499646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20773077..20862801hg38UCSC Ensembl
Innerchr16:20784399..20874123hg19UCSC Ensembl
Innerchr16:20691900..20781624hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3889725
hg1989725
hg1889725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050009
Supporting Variants
Samples
Known GenesACSM3, DCUN1D3, ERI2, LOC81691
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3548051
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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