A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586619



Internal ID16027342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63737451..63738644hg38UCSC Ensembl
Innerchr20:62368804..62369997hg19UCSC Ensembl
Innerchr20:61839248..61840441hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381194
hg191194
hg181194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7678n54
Supporting Variantsnssv943847
Samples
Known GenesLIME1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586619
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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