A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025481



Internal ID19114699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:79194058..79266992hg38UCSC Ensembl
Innerchr8:80106293..80179227hg19UCSC Ensembl
Innerchr8:80268848..80341782hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3872935
hg1972935
hg1872935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689583
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)nsv1025481
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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