A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7492n100



Internal ID22793579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28643635..28813879hg38UCSC Ensembl
chr9:28643633..28813877hg19UCSC Ensembl
chr9:28633633..28803877hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38170245
hg19170245
hg18170245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021215, nsv1026302, nsv1020046
Samples
Known GenesLINGO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7492n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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