A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7350n100



Internal ID22793437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:162695..399040hg38UCSC Ensembl
chr9:162695..399040hg19UCSC Ensembl
chr9:152695..389040hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38236346
hg19236346
hg18236346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025542, nsv1026550, nsv1015936, nsv1021696, nsv1021611, nsv1024500, nsv1022226, nsv1018804, nsv1031702
Samples
Known GenesC9orf66, CBWD1, DOCK8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7350n100
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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