A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024876



Internal ID18767407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102500557..102564430hg38UCSC Ensembl
Innerchr8:103512785..103576658hg19UCSC Ensembl
Innerchr8:103581961..103645834hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3863874
hg1963874
hg1863874
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691257
Samples
Known GenesODF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024876
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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