A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598880



Internal ID6639145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181001654..181009931hg38UCSC Ensembl
chr3:180719442..180727719hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg388278
hg198278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv958e214
Supporting Variantsessv11251117, essv11251118
SamplesHG02323, HG03354
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598880
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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