A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058853



Internal ID19148072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33108213..33163485hg38UCSC Ensembl
Innerchr20:31696019..31751291hg19UCSC Ensembl
Innerchr20:31159680..31214952hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3855273
hg1955273
hg1855273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737193
Samples
Known GenesBPIFB4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058853
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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