A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1326e199



Internal ID22759099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14686670..14688751hg38UCSC Ensembl
chr9:14686668..14688749hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382082
hg192082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2664275, esv2665296
SamplesNA19703, NA18508, NA19914, NA18486, NA19377, NA20356, NA19107, NA18923, NA19916, NA18916, NA18498, NA18874, NA18868, NA19238, NA19172, NA20127, NA18908, NA18867, NA19451, HG01124, NA20126, NA18871, NA18907, NA18499, NA18858, NA19108, NA19147, NA19467, NA19818, NA19093, NA18522, NA18487
Known GenesZDHHC21
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1326e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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