A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625225



Internal ID15848761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:33455712..33457986hg38UCSC Ensembl
Outerchr20:32043518..32045792hg19UCSC Ensembl
Outerchr20:31507179..31509453hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg382275
hg192275
hg182275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512612
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)nssv625225
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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