A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7726n100



Internal ID22793813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135247933..135426111hg38UCSC Ensembl
chr9:138139779..138317957hg19UCSC Ensembl
chr9:137279600..137457778hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38178179
hg19178179
hg18178179
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041292, nsv1054284, nsv1039442, nsv1043612, nsv1041700, nsv1038821, nsv1044581, nsv1039228, nsv1048149, nsv1039832, nsv1036928, nsv1047318, nsv1043901, nsv1045847, nsv1035302, nsv1041990, nsv1044512
Samples
Known GenesC9orf62
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7726n100
Frequency
Sample Size11257
Observed Gain77
Observed Loss0
Observed Complex0
Frequencyn/a


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