A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7224n100



Internal ID22793311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53042643..53080343hg38UCSC Ensembl
chr8:53955203..53992903hg19UCSC Ensembl
chr8:54117756..54155456hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3837701
hg1937701
hg1837701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018298, nsv1033198, nsv1016426, nsv1025416, nsv1028737, nsv1018542, nsv1030839, nsv1033851
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)dgv7224n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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