A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673134



Internal ID9939239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9708657..9709387hg38UCSC Ensembl
chr3:9750341..9751071hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6514882, essv5699169, essv5460401
SamplesHG00361, HG00284, HG00366
Known GenesCPNE9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673134
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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