A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11091748



Internal ID4509153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104122812..104209900hg38UCSC Ensembl
chr3:103841656..103928744hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3887089
hg1987089
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597239
Supporting Variants
SamplesHG04006
Known GenesMIR548A3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11091748
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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