A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603538



Internal ID6990569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186639347..186667237hg38UCSC Ensembl
Innerchr4:186639347..186667237hg38UCSC Ensembl
Outerchr4:186638847..186667737hg38UCSC Ensembl
chr4:187560501..187588391hg19UCSC Ensembl
Innerchr4:187560501..187588391hg19UCSC Ensembl
Outerchr4:187560001..187588891hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3827891
hg1927891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11746389
SamplesHG03702
Known GenesFAT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603538
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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