A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1245n145



Internal ID22814261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95503288..95514540hg38UCSC Ensembl
chr9:98265570..98276822hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3811253
hg1911253
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113724, nsv3117730, nsv3117170
Samplessample306, sample243, sample273
Known GenesPTCH1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1245n145
Frequency
Sample Size467
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer