A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611451



Internal ID16398860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:65179929..65182185hg38UCSC Ensembl
Innerchr8:66092164..66094420hg19UCSC Ensembl
Innerchr8:66254718..66256974hg18UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg382257
hg192257
hg182257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12185n54
Supporting Variantsnssv1115727
Samples
Known GenesLINC00251
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611451
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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