A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031436



Internal ID18773970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:22458146..22546143hg38UCSC Ensembl
Innerchr8:22315659..22403656hg19UCSC Ensembl
Innerchr8:22371604..22459601hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3887998
hg1987998
hg1887998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7137n100
Supporting Variantsnssv3685366
Samples
Known GenesPPP3CC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031436
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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