A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626282



Internal ID15849815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35249582..35250059hg38UCSC Ensembl
Outerchr22:35235597..35253605hg38UCSC Ensembl
Innerchr22:35645575..35646052hg19UCSC Ensembl
Outerchr22:35631590..35649598hg19UCSC Ensembl
Innerchr22:33975575..33976052hg18UCSC Ensembl
Outerchr22:33961590..33979598hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3818009
hg1918009
hg1818009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511647
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)nssv626282
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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