A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv267n97



Internal ID22815664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103186207..103237281hg38UCSC Ensembl
chr7:102826654..102877728hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3851075
hg1951075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156705, nsv1156706
Samples
Known GenesDPY19L2P2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv267n97
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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