A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6178086



Internal ID8793655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27404242..27405312hg38UCSC Ensembl
Outerchr6:27404085..27405465hg38UCSC Ensembl
Innerchr6:27372021..27373091hg19UCSC Ensembl
Outerchr6:27371864..27373244hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381381
hg191381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657463
Supporting Variants
SamplesHG00237
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6178086
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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