A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5632141



Internal ID9018300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:19092276..19097374hg38UCSC Ensembl
chr3:19133768..19138866hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385099
hg195099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673521
Supporting Variants
SamplesHG00635
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5632141
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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