A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667426



Internal ID9586845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29397143..29417723hg38UCSC Ensembl
chr6:29364920..29385500hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3820581
hg1920581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6534603, essv6097428, essv6469021, essv6043089, essv5450150, essv5472586, essv5795737
SamplesNA19248, NA20787, NA20761, NA18635, NA18536, HG00584, NA20581
Known GenesOR12D2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667426
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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