A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028876



Internal ID19118095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:5749554..6352939hg38UCSC Ensembl
Innerchr8:5607076..6210460hg19UCSC Ensembl
Innerchr8:5594484..6197868hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38603386
hg19603385
hg18603385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3675596
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028876
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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