A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586618



Internal ID16027341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63736025..63740688hg38UCSC Ensembl
Innerchr20:62367377..62372041hg19UCSC Ensembl
Innerchr20:61837821..61842485hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384664
hg194665
hg184665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv943846
Samples
Known GenesLIME1, SLC2A4RG, ZGPAT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586618
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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