A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586625



Internal ID16027348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63737451..63741603hg38UCSC Ensembl
Innerchr20:62368804..62372956hg19UCSC Ensembl
Innerchr20:61839248..61843400hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384153
hg194153
hg184153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7680n54
Supporting Variantsnssv943855
Samples
Known GenesLIME1, SLC2A4RG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586625
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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