A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511509



Internal ID15850934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:72271812..72272637hg38UCSC Ensembl
Outerchr13:72264171..72273500hg38UCSC Ensembl
Innerchr13:72845950..72846775hg19UCSC Ensembl
Outerchr13:72838309..72847638hg19UCSC Ensembl
Innerchr13:71743951..71744776hg18UCSC Ensembl
Outerchr13:71736310..71745639hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg389330
hg199330
hg189330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626128
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)nsv511509
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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