A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610773



Internal ID16051496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:22696108..22721359hg38UCSC Ensembl
Innerchr8:22553621..22578872hg19UCSC Ensembl
Innerchr8:22609566..22634817hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3825252
hg1925252
hg1825252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12056n54
Supporting Variantsnssv1107477
Samples
Known GenesPEBP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610773
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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