A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665731



Internal ID9931836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:88299474..88411352hg38UCSC Ensembl
Innerchr3:88348624..88460502hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38111879
hg19111879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6103080
SamplesNA12878
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665731
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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