A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7458n100



Internal ID22793545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13301945..13340591hg38UCSC Ensembl
chr9:13301944..13340590hg19UCSC Ensembl
chr9:13291944..13330590hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3838647
hg1938647
hg1838647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028113, nsv1022278, nsv1016717, nsv1015235
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)dgv7458n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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