A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597488



Internal ID6984629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116169351..116183784hg38UCSC Ensembl
chr3:115888198..115902631hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3814434
hg1914434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv923e214
Supporting Variantsessv11111213, essv11111214
SamplesHG01953, NA20799
Known GenesLSAMP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597488
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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