A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7305n100



Internal ID22793392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122449335..122467565hg38UCSC Ensembl
chr8:123461574..123479804hg19UCSC Ensembl
chr8:123530755..123548985hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3818231
hg1918231
hg1818231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021597, nsv1015911
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)dgv7305n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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