A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626843



Internal ID15850376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:38109928..38110298hg38UCSC Ensembl
Outerchr22:38505935..38506305hg19UCSC Ensembl
Outerchr22:36835881..36836251hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381435
hg191435
hg181435
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513591
Supporting Variants
Samples1
Known GenesBAIAP2L2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626843
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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