A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025583



Internal ID19114801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:22902748..22918793hg38UCSC Ensembl
Innerchr8:22760261..22776306hg19UCSC Ensembl
Innerchr8:22816206..22832251hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3816046
hg1916046
hg1816046
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685370
Samples
Known GenesPEBP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025583
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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