A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597256



Internal ID6972190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104541962..104731289hg38UCSC Ensembl
chr3:104260806..104450133hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38189328
hg19189328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11092069
SamplesNA18966
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597256
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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