A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585414



Internal ID16372823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:10005758..10050283hg38UCSC Ensembl
Innerchr20:9986406..10030931hg19UCSC Ensembl
Innerchr20:9934406..9978931hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3844526
hg1944526
hg1844526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937959
Samples
Known GenesANKEF1, SNAP25-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585414
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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