A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598878



Internal ID6972396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180927315..180934574hg38UCSC Ensembl
chr3:180645103..180652362hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg387260
hg197260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11251114, essv11251115
SamplesNA18639, HG02090
Known GenesFXR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598878
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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