A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv256n97



Internal ID22815653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110065139..110094225hg38UCSC Ensembl
chr6:110386342..110415428hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3829087
hg1929087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156571, nsv1156570
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv256n97
Frequency
Sample Size131
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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