A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612489



Internal ID16399898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:137085326..137123693hg38UCSC Ensembl
Innerchr8:138097569..138135936hg19UCSC Ensembl
Innerchr8:138166751..138205118hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3838368
hg1938368
hg1838368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1122468
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612489
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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