A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1246n145



Internal ID22814262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95504459..95511948hg38UCSC Ensembl
chr9:98266741..98274230hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg387490
hg197490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112915, nsv3112342, nsv3114675
Samplessample98, sample208, sample229
Known GenesPTCH1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1246n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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