A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5929074



Internal ID9724243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14343553..14350665hg38UCSC Ensembl
chr3:14385053..14392165hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg387113
hg197113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670533
Supporting Variants
SamplesNA19474
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5929074
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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