A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7498n100



Internal ID20159114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28847172..29183431hg38UCSC Ensembl
chr9:28847170..29183429hg19UCSC Ensembl
chr9:28837170..29173429hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38336260
hg19336260
hg18336260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020807, nsv1031655
Samples
Known GenesLINGO2, MIR873, MIR876
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7498n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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