A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7490n100



Internal ID22793577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28187705..28347681hg38UCSC Ensembl
chr9:28187703..28347679hg19UCSC Ensembl
chr9:28177703..28337679hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38159977
hg19159977
hg18159977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021373, nsv1016994
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)dgv7490n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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