A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7322n100



Internal ID22793409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133151196..133172768hg38UCSC Ensembl
chr8:134163440..134185012hg19UCSC Ensembl
chr8:134232622..134254194hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3821573
hg1921573
hg1821573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016608, nsv1018358, nsv1024676
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)dgv7322n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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