A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667016



Internal ID9933121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32058155..32061494hg38UCSC Ensembl
chr6:32025932..32029271hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg383340
hg193340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1099e199
Supporting Variantsessv5952494, essv6523312, essv6009104
SamplesNA19372, HG01101, HG01375
Known GenesTNXB
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667016
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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