A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7694n100



Internal ID22793781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103255004..103290151hg38UCSC Ensembl
chr9:106017286..106052433hg19UCSC Ensembl
chr9:105057107..105092254hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3835148
hg1935148
hg1835148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043740, nsv1043051
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)dgv7694n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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