A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668033



Internal ID9934138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194990097..194993585hg38UCSC Ensembl
chr3:194710826..194714314hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg383489
hg193489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6008903, essv6370415, essv6141148, essv6501600, essv5753607, essv6185800
SamplesNA11920, HG00330, NA12282, HG00266, HG00366, HG00345
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668033
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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