A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7269n100



Internal ID22793356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93269582..93303098hg38UCSC Ensembl
chr8:94281810..94315326hg19UCSC Ensembl
chr8:94350986..94384502hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3833517
hg1933517
hg1833517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033372, nsv1020914
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)dgv7269n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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