A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5420537



Internal ID9759985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15272568..15272696hg38UCSC Ensembl
chr3:15314075..15314203hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660869
Supporting Variants
SamplesNA19713
Known GenesSH3BP5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5420537
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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