A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512609



Internal ID15852034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:32174651..32177665hg38UCSC Ensembl
Outerchr20:30762454..30765468hg19UCSC Ensembl
Outerchr20:30226115..30229129hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg383015
hg193015
hg183015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625222
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)nsv512609
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer