A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585774



Internal ID16373183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26125809..26337643hg38UCSC Ensembl
Innerchr20:26106445..26318279hg19UCSC Ensembl
Innerchr20:26054445..26266279hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38211835
hg19211835
hg18211835
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939003
Samples
Known GenesLOC284801, MIR663A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585774
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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