A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586703



Internal ID16374112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63964886..64095388hg38UCSC Ensembl
Innerchr20:62596239..62726741hg19UCSC Ensembl
Innerchr20:62066683..62197185hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38130503
hg19130503
hg18130503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944092, nssv944091
Samples
Known GenesC20orf201, LINC00176, MIR6813, OPRL1, PRPF6, RGS19, SAMD10, SOX18, TCEA2, ZNF512B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586703
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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