A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586176



Internal ID16026899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:49537207..49561676hg38UCSC Ensembl
Innerchr20:48153744..48178213hg19UCSC Ensembl
Innerchr20:47587151..47611620hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3824470
hg1924470
hg1824470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv940982
Samples
Known GenesPTGIS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586176
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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