A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676841



Internal ID9942946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103355059..103368560hg38UCSC Ensembl
chr3:103073903..103087404hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3813502
hg1913502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6196928
SamplesNA18999
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676841
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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