A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585787



Internal ID16373196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26276714..26337643hg38UCSC Ensembl
Innerchr20:26257350..26318279hg19UCSC Ensembl
Innerchr20:26205350..26266279hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3860930
hg1960930
hg1860930
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7527n54
Supporting Variantsnssv939023, nssv939024, nssv939025, nssv939020, nssv939022, nssv939021
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585787
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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