A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586812



Internal ID16374221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64117527..64119011hg38UCSC Ensembl
Innerchr20:62748880..62750364hg19UCSC Ensembl
Innerchr20:62219324..62220808hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381485
hg191485
hg181485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7716n54
Supporting Variantsnssv944547
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586812
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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