A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586486



Internal ID16027209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62315508..62378340hg38UCSC Ensembl
Innerchr20:60890564..60953396hg19UCSC Ensembl
Innerchr20:60323959..60386791hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3862833
hg1962833
hg1862833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7650n54
Supporting Variantsnssv1151407
SamplesNINDS_119
Known GenesLAMA5, MIR4758
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586486
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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