A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585162



Internal ID16372571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:82603..120721hg38UCSC Ensembl
Innerchr20:63244..101362hg19UCSC Ensembl
Innerchr20:11244..49362hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3838119
hg1938119
hg1838119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv935226
Samples
Known GenesDEFB125
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585162
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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