A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7363n100



Internal ID22793450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:525037..816742hg38UCSC Ensembl
chr9:525037..816742hg19UCSC Ensembl
chr9:515037..806742hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38291706
hg19291706
hg18291706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031342, nsv1018759, nsv1019676, nsv1021488, nsv1033964
Samples
Known GenesKANK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7363n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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