A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603461



Internal ID6990492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184558642..184559913hg38UCSC Ensembl
Innerchr4:184558656..184559900hg38UCSC Ensembl
Outerchr4:184558629..184559927hg38UCSC Ensembl
chr4:185479796..185481067hg19UCSC Ensembl
Innerchr4:185479810..185481054hg19UCSC Ensembl
Outerchr4:185479783..185481081hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381272
hg191272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11733367, essv11733366
SamplesNA07347, HG01536
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603461
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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