A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511626



Internal ID15851051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:44677392..44679373hg38UCSC Ensembl
Outerchr20:44667497..44680637hg38UCSC Ensembl
Innerchr20:43306033..43308014hg19UCSC Ensembl
Outerchr20:43296138..43309278hg19UCSC Ensembl
Innerchr20:42739447..42741428hg18UCSC Ensembl
Outerchr20:42729552..42742692hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3813141
hg1913141
hg1813141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626259
Samples1
Known GenesLOC79015
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511626
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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