A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658061



Internal ID9924166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98150966..98203575hg38UCSC Ensembl
Outerchr3:98150932..98203610hg38UCSC Ensembl
Innerchr3:97869810..97922419hg19UCSC Ensembl
Outerchr3:97869776..97922454hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3852679
hg1952679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv872e199
Supporting Variantsessv5552615
SamplesNA18522
Known GenesOR5H15
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658061
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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