A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5938936



Internal ID9192936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82800764..82801993hg38UCSC Ensembl
chr6:83510481..83511710hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381230
hg191230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658482
Supporting Variants
SamplesHG01489
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5938936
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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