A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625270



Internal ID15502120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:26771925..26773877hg38UCSC Ensembl
Outerchr22:27167888..27169840hg19UCSC Ensembl
Outerchr22:25497888..25499840hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg381953
hg191953
hg181953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512652
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625270
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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