A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6009104



Internal ID9106267
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 Flag1
Merged StatusS
Merged Variantsesv2667016
Supporting Variants
SamplesHG01101
Known GenesTNXB
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6009104
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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