A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6813n100



Internal ID22792900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:2183328..2674095hg38UCSC Ensembl
chr8:2131525..2531603hg19UCSC Ensembl
chr8:2118932..2519010hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38490768
hg19400079
hg18400079
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031221, nsv1023252
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)dgv6813n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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