A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626842



Internal ID15850375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:37226812..37226876hg38UCSC Ensembl
Outerchr22:37622852..37622916hg19UCSC Ensembl
Outerchr22:35952798..35952862hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38873
hg19873
hg18873
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513590
Supporting Variants
Samples1
Known GenesRAC2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626842
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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