A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7454n100



Internal ID22793541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12280677..12452015hg38UCSC Ensembl
chr9:12280677..12452015hg19UCSC Ensembl
chr9:12270677..12442015hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38171339
hg19171339
hg18171339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015495, nsv1034794
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)dgv7454n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer