A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6207232



Internal ID9184635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:236689..236894hg38UCSC Ensembl
chr3:278372..278577hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663135
Supporting Variants
SamplesNA19377
Known GenesCHL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6207232
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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