A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5568655



Internal ID9543256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158892891..158897617hg38UCSC Ensembl
chr6:159313923..159318649hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384727
hg194727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677655
Supporting Variants
SamplesNA19075
Known GenesC6orf99
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5568655
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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