A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586629



Internal ID16374038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63737667..63739900hg38UCSC Ensembl
Innerchr20:62369020..62371253hg19UCSC Ensembl
Innerchr20:61839464..61841697hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382234
hg192234
hg182234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7682n54
Supporting Variantsnssv943859
Samples
Known GenesLIME1, SLC2A4RG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586629
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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