A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6156197



Internal ID9021942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31305293..31310186hg38UCSC Ensembl
chr3:31346785..31351678hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg384894
hg194894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666780
Supporting Variants
SamplesHG00641
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6156197
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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