A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv298n97



Internal ID22815695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30616488..30708218hg38UCSC Ensembl
chr9:30616486..30708216hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3891731
hg1991731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154476, nsv1154477
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv298n97
Frequency
Sample Size131
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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