A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661920



Internal ID9928025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15761710..15774686hg38UCSC Ensembl
chr6:15761941..15774917hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3812977
hg1912977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5866369
SamplesNA19393
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661920
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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