A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586728



Internal ID16374137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64048542..64049671hg38UCSC Ensembl
Innerchr20:62679895..62681024hg19UCSC Ensembl
Innerchr20:62150339..62151468hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381130
hg191130
hg181130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944153
Samples
Known GenesSOX18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586728
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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