A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6478198



Internal ID9455601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43197208..43197645hg38UCSC Ensembl
chr6:43164946..43165383hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2671960
Supporting Variants
SamplesNA19453
Known GenesCUL9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6478198
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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