A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603227



Internal ID6990259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174384984..174401271hg38UCSC Ensembl
Innerchr4:174384984..174401271hg38UCSC Ensembl
Outerchr4:174384484..174401771hg38UCSC Ensembl
chr4:175306135..175322422hg19UCSC Ensembl
Innerchr4:175306135..175322422hg19UCSC Ensembl
Outerchr4:175305635..175322922hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3816288
hg1916288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11710112, essv11710111, essv11710114, essv11710109, essv11710113, essv11710110, essv11710108
SamplesHG02658, HG03652, HG04033, HG03743, HG02660, HG03977, HG03890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603227
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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