A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7385n100



Internal ID22793472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5375365..5396960hg38UCSC Ensembl
chr9:5375365..5396960hg19UCSC Ensembl
chr9:5365365..5386960hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3821596
hg1921596
hg1821596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024748, nsv1017774
Samples
Known GenesPLGRKT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7385n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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