A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598284



Internal ID6638549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155760377..155780857hg38UCSC Ensembl
chr3:155478166..155498646hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3820481
hg1920481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11191895
SamplesNA21088
Known GenesC3orf33
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598284
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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