A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612427



Internal ID16399836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136685592..136834818hg38UCSC Ensembl
Innerchr8:137697835..137847061hg19UCSC Ensembl
Innerchr8:137767017..137916243hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38149227
hg19149227
hg18149227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1122406
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612427
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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