A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7481n100



Internal ID22793568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24554120..24684865hg38UCSC Ensembl
chr9:24554118..24684863hg19UCSC Ensembl
chr9:24544118..24674863hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38130746
hg19130746
hg18130746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025979, nsv1032634
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)dgv7481n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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