A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586399



Internal ID16373808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61124043..61132208hg38UCSC Ensembl
Innerchr20:59699099..59707264hg19UCSC Ensembl
Innerchr20:59132494..59140659hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg388166
hg198166
hg188166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151397
SamplesNINDS_23
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586399
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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