A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv248n97



Internal ID22815645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40095143..40135568hg38UCSC Ensembl
chr6:40062882..40103307hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3840426
hg1940426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156497, nsv1156498
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv248n97
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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