A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7278n100



Internal ID20158894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102664742..102716969hg38UCSC Ensembl
chr8:103676970..103729197hg19UCSC Ensembl
chr8:103746146..103798373hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3852228
hg1952228
hg1852228
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018625, nsv1026755
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)dgv7278n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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