A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5474734



Internal ID9096166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72130880..72131369hg38UCSC Ensembl
chr3:72180031..72180520hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663888
Supporting Variants
SamplesHG01079
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5474734
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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