A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1354e199



Internal ID22759127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82257053..82264437hg38UCSC Ensembl
chr9:84871968..84879352hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg387385
hg197385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2668434, esv2661936
SamplesNA19651
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1354e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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