A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611241



Internal ID16398650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:46193535..47036078hg38UCSC Ensembl
Innerchr8:47105157..47947701hg19UCSC Ensembl
Innerchr8:47224322..48066866hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38842544
hg19842545
hg18842545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1114133
Samples
Known GenesLINC00293
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611241
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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