A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7412n100



Internal ID22793499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11582831..11934365hg38UCSC Ensembl
chr9:11582831..11934365hg19UCSC Ensembl
chr9:11572831..11924365hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38351535
hg19351535
hg18351535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015379, nsv1019320, nsv1020402
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)dgv7412n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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