A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7398n100



Internal ID22793485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9796577..9822041hg38UCSC Ensembl
chr9:9796577..9822041hg19UCSC Ensembl
chr9:9786577..9812041hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3825465
hg1925465
hg1825465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018188, nsv1018895, nsv1025772, nsv1022667, nsv1034821
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)dgv7398n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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