A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7376n100



Internal ID22793463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2253741..2415423hg38UCSC Ensembl
chr9:2253741..2415423hg19UCSC Ensembl
chr9:2243741..2405423hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38161683
hg19161683
hg18161683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016677, nsv1016401
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)dgv7376n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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