A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586612



Internal ID16027335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63686867..63702570hg38UCSC Ensembl
Innerchr20:62318220..62333922hg19UCSC Ensembl
Innerchr20:61788664..61804366hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3815704
hg1915703
hg1815703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7676n54
Supporting Variantsnssv943840
Samples
Known GenesARFRP1, RTEL1, RTEL1-TNFRSF6B, TNFRSF6B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586612
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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