A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6820n100



Internal ID22792907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:2308620..2738156hg38UCSC Ensembl
chr8:2254675..2595684hg19UCSC Ensembl
chr8:2242082..2583091hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38429537
hg19341010
hg18341010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026105, nsv1016370, nsv1017329, nsv1028602, nsv1025156, nsv1021273, nsv1025592, nsv1028633, nsv1025628, nsv1032782, nsv1021589, nsv1031776
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)dgv6820n100
Frequency
Sample Size11257
Observed Gain53
Observed Loss0
Observed Complex0
Frequencyn/a


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