A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5968094



Internal ID9806761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85834814..85862731hg38UCSC Ensembl
chr6:86544532..86572449hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3827918
hg1927918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665695
Supporting Variants
SamplesNA19908
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5968094
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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