A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673521



Internal ID9939626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:19092276..19097374hg38UCSC Ensembl
chr3:19133768..19138866hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385099
hg195099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5416008, essv5632141
SamplesHG00635, HG00578
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673521
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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