A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586617



Internal ID16027340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63736025..63738644hg38UCSC Ensembl
Innerchr20:62367377..62369997hg19UCSC Ensembl
Innerchr20:61837821..61840441hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382620
hg192621
hg182621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7677n54
Supporting Variantsnssv943845
Samples
Known GenesLIME1, ZGPAT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586617
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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