A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585163



Internal ID16372572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:82603..127687hg38UCSC Ensembl
Innerchr20:63244..108328hg19UCSC Ensembl
Innerchr20:11244..56328hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3845085
hg1945085
hg1845085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv935227
Samples
Known GenesDEFB125
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585163
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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