A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599087



Internal ID6986135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:191119944..191159248hg38UCSC Ensembl
chr3:190837733..190877037hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3839305
hg1939305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11269498
SamplesHG01920
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599087
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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