A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612418



Internal ID16399827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675987..136837820hg38UCSC Ensembl
Innerchr8:137688230..137850063hg19UCSC Ensembl
Innerchr8:137757412..137919245hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38161834
hg19161834
hg18161834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1156189
SamplesHGDP00670
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612418
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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