A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586816



Internal ID16374225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64117743..64119126hg38UCSC Ensembl
Innerchr20:62749096..62750479hg19UCSC Ensembl
Innerchr20:62219540..62220923hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381384
hg191384
hg181384
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7716n54
Supporting Variantsnssv944558, nssv944559
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586816
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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