A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11093206



Internal ID5453530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105010980..105071172hg38UCSC Ensembl
chr3:104729824..104790016hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3860193
hg1960193
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597270
Supporting Variants
SamplesNA18966
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11093206
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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