A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1281e199



Internal ID22759054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36576863..36581216hg38UCSC Ensembl
chr8:36434381..36438734hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg384354
hg194354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2677849, esv2661333
SamplesNA18546
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1281e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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