A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659952



Internal ID9926057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19175436..19180472hg38UCSC Ensembl
chr6:19175667..19180703hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385037
hg195037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5952847, essv5589320, essv5827182
SamplesNA18532, HG00463, NA19004
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659952
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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