A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512901



Internal ID15852323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:170052539..170053183hg38UCSC Ensembl
Outerchr6:170367763..170368407hg19UCSC Ensembl
Outerchr6:170209688..170210332hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38919
hg19919
hg18919
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625547
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)nsv512901
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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