A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511310



Internal ID15850735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:45005092..45014303hg38UCSC Ensembl
Outerchr5:45003191..45037924hg38UCSC Ensembl
Innerchr5:45005194..45014405hg19UCSC Ensembl
Outerchr5:45003293..45038026hg19UCSC Ensembl
Innerchr5:45040951..45050162hg18UCSC Ensembl
Outerchr5:45039050..45073783hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3834734
hg1934734
hg1834734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625343
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511310
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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