A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7276n100



Internal ID22793363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101371556..101396319hg38UCSC Ensembl
chr8:102383784..102408547hg19UCSC Ensembl
chr8:102452960..102477723hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3824764
hg1924764
hg1824764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021027, nsv1025254, nsv1021737, nsv1031216
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)dgv7276n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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