A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598260



Internal ID6985396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154814460..154973310hg38UCSC Ensembl
chr3:154532249..154691099hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38158851
hg19158851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11190156, essv11190157
SamplesHG00406, NA21088
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598260
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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