A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7211n100



Internal ID22793298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47250820..47334731hg38UCSC Ensembl
chr8:48163412..48247297hg19UCSC Ensembl
chr8:48325965..48409850hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3883912
hg1983886
hg1883886
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030486, nsv1031331, nsv1032993, nsv1023786
Samples
Known GenesSPIDR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7211n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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