A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1332e199



Internal ID22759105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27629767..27635175hg38UCSC Ensembl
chr9:27629765..27635173hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg385409
hg195409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2659192, esv2674602
SamplesHG00120
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1332e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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