A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062857



Internal ID18805388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33032555..33066287hg38UCSC Ensembl
Innerchr20:31620361..31654093hg19UCSC Ensembl
Innerchr20:31084022..31117754hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3833733
hg1933733
hg1833733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584738
Samples
Known GenesBPIFB3, BPIFB6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062857
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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