A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625241



Internal ID15848777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:64116186..64119475hg38UCSC Ensembl
Outerchr20:62747539..62750828hg19UCSC Ensembl
Outerchr20:62217983..62221272hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg383290
hg193290
hg183290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512627
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625241
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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