A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7698n100



Internal ID20159314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105773532..105969062hg38UCSC Ensembl
chr9:108535813..108731343hg19UCSC Ensembl
chr9:107575634..107771164hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38195531
hg19195531
hg18195531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041073, nsv1052684
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7698n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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