A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6192108



Internal ID9322387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106110005..106112772hg38UCSC Ensembl
chr3:105828852..105831619hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg382768
hg192768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672726
Supporting Variants
SamplesNA18516
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6192108
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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