A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7483n100



Internal ID22793570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:25251851..25353889hg38UCSC Ensembl
chr9:25251849..25353887hg19UCSC Ensembl
chr9:25241849..25343887hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38102039
hg19102039
hg18102039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024204, nsv1032112, nsv1029572, nsv1022440, nsv1026386, nsv1032258
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)dgv7483n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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