A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv265n97



Internal ID22815662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66211052..66238935hg38UCSC Ensembl
chr7:65676039..65703922hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3827884
hg1927884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156681, nsv1156682
Samples
Known GenesTPST1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv265n97
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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