A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7389n100



Internal ID22793476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6548393..6708345hg38UCSC Ensembl
chr9:6548393..6708345hg19UCSC Ensembl
chr9:6538393..6698345hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38159953
hg19159953
hg18159953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018870, nsv1034936
Samples
Known GenesGLDC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7389n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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