A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599651



Internal ID6986696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11624300..11818899hg38UCSC Ensembl
chr4:11625924..11820523hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38194600
hg19194600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv985e214
Supporting Variantsessv11357080, essv11357079
SamplesHG00524, HG04080
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599651
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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