A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599758



Internal ID6986803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16421889..16427961hg38UCSC Ensembl
chr4:16423512..16429584hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg386073
hg196073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv990e214
Supporting Variantsessv11360371, essv11360372, essv11360373
SamplesHG01443, HG00330, NA11831
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599758
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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