A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611852



Internal ID16399261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:107491474..107493626hg38UCSC Ensembl
Innerchr8:108503702..108505854hg19UCSC Ensembl
Innerchr8:108572878..108575030hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg382153
hg192153
hg182153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12253n54
Supporting Variantsnssv1118244
Samples
Known GenesANGPT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611852
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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