A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5998749



Internal ID8899334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85663245..85664210hg38UCSC Ensembl
chr6:86372963..86373928hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38966
hg19966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675124
Supporting Variants
SamplesHG00346
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5998749
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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