A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5921097



Internal ID9810502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:115382794..115397195hg38UCSC Ensembl
chr6:115703958..115718359hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3814402
hg1914402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677989
Supporting Variants
SamplesNA19916
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5921097
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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