A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6290697



Internal ID9383830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14379765..14380910hg38UCSC Ensembl
chr6:14379996..14381141hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381146
hg191146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666824
Supporting Variants
SamplesNA18576
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6290697
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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