A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659549



Internal ID9925654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9318166..9327441hg38UCSC Ensembl
chr3:9359850..9369125hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg389276
hg199276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5837163, essv6136649, essv5937842, essv5779239, essv5443100, essv6351415
SamplesHG00335, HG00325, HG00309, HG00313, HG00176, NA12006
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659549
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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