A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586813



Internal ID16374222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64117527..64119126hg38UCSC Ensembl
Innerchr20:62748880..62750479hg19UCSC Ensembl
Innerchr20:62219324..62220923hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381600
hg191600
hg181600
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7716n54
Supporting Variantsnssv944551, nssv944549, nssv944552, nssv944550, nssv944548
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586813
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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