A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626263



Internal ID15849796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17240023..17240912hg38UCSC Ensembl
Outerchr21:17238161..17251751hg38UCSC Ensembl
Innerchr21:18612341..18613230hg19UCSC Ensembl
Outerchr21:18610479..18624069hg19UCSC Ensembl
Innerchr21:17534212..17535101hg18UCSC Ensembl
Outerchr21:17532350..17545940hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3813591
hg1913591
hg1813591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511630
Supporting Variants
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)nssv626263
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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