A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5898228



Internal ID9566072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96252451..96253615hg38UCSC Ensembl
chr6:96700327..96701491hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381165
hg191165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660350
Supporting Variants
SamplesNA19114
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5898228
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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