A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584732



Internal ID18536327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:32469234..33355029hg38UCSC Ensembl
Innerchr20:31057037..31942835hg19UCSC Ensembl
Innerchr20:30520698..31406496hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38885796
hg19885799
hg18885799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056411
Supporting Variants
Samples
Known GenesBPIFA1, BPIFA2, BPIFA3, BPIFA4P, BPIFB1, BPIFB2, BPIFB3, BPIFB4, BPIFB6, C20orf112, C20orf203, COMMD7, DNMT3B, LOC149950, MAPRE1, SUN5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584732
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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