A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586165



Internal ID16026888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:48128545..48491735hg38UCSC Ensembl
Innerchr20:46757288..47119981hg19UCSC Ensembl
Innerchr20:46190695..46553388hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38363191
hg19362694
hg18362694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv940972
Samples
Known GenesLINC00494
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586165
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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