A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6526562



Internal ID8990829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180110108..180115553hg38UCSC Ensembl
chr3:179827896..179833341hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg385446
hg195446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676698
Supporting Variants
SamplesHG00584
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6526562
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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