A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7405n100



Internal ID22793492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10439300..10504304hg38UCSC Ensembl
chr9:10439300..10504304hg19UCSC Ensembl
chr9:10429300..10494304hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3865005
hg1965005
hg1865005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022061, nsv1028702
Samples
Known GenesPTPRD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7405n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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