A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1339e201



Internal ID6313850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:139430215..139430551hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsesv2741141, esv2742236
SamplesSSM043, SSM083
Known GenesNOTCH1
Method
Analysis
Platform
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)dgv1339e201
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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