A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512655



Internal ID15852080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:35736630..35738574hg38UCSC Ensembl
Outerchr22:36132677..36134621hg19UCSC Ensembl
Outerchr22:34462623..34464567hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381945
hg191945
hg181945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625273
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)nsv512655
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer