A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7491n100



Internal ID22793578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28587776..28768828hg38UCSC Ensembl
chr9:28587774..28768826hg19UCSC Ensembl
chr9:28577774..28758826hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38181053
hg19181053
hg18181053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022010, nsv1026123, nsv1033016, nsv1030476, nsv1021668, nsv1032891, nsv1028793, nsv1025773, nsv1017704
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)dgv7491n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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