A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626271



Internal ID15849804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38899541..38902528hg38UCSC Ensembl
Outerchr22:38895853..38910075hg38UCSC Ensembl
Innerchr22:39295546..39298533hg19UCSC Ensembl
Outerchr22:39291858..39306080hg19UCSC Ensembl
Innerchr22:37625492..37628479hg18UCSC Ensembl
Outerchr22:37621804..37636026hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3814223
hg1914223
hg1814223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511637
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)nssv626271
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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