A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625621



Internal ID15849154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:133959584..133960090hg38UCSC Ensembl
Outerchr8:134971827..134972333hg19UCSC Ensembl
Outerchr8:135041009..135041515hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg381076
hg191076
hg181076
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512968
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)nssv625621
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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