A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7708n100



Internal ID20159324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116663365..116741547hg38UCSC Ensembl
chr9:119425644..119503826hg19UCSC Ensembl
chr9:118465465..118543647hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3878183
hg1978183
hg1878183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036431, nsv1051953
Samples
Known GenesASTN2, TRIM32
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7708n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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