A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595587



Internal ID6982905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24704076..24784823hg38UCSC Ensembl
chr3:24745567..24826314hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3880748
hg1980748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv878e214
Supporting Variantsessv10950164, essv10950163, essv10950165
SamplesNA19035, NA19321, NA18620
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595587
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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