A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7437n100



Internal ID22793524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11964248..12253242hg38UCSC Ensembl
chr9:11964248..12253242hg19UCSC Ensembl
chr9:11954248..12243242hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38288995
hg19288995
hg18288995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024622, nsv1020196, nsv1031356
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)dgv7437n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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