A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1379e199



Internal ID22759152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128447961..128454621hg38UCSC Ensembl
chr9:131210240..131216900hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386661
hg196661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672041, esv2671410
SamplesHG00577, HG00595
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1379e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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