A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603344



Internal ID6990376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:178946665..179154695hg38UCSC Ensembl
Innerchr4:178947165..179154195hg38UCSC Ensembl
Outerchr4:178945665..179155695hg38UCSC Ensembl
chr4:179867819..180075849hg19UCSC Ensembl
Innerchr4:179868319..180075349hg19UCSC Ensembl
Outerchr4:179866819..180076849hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38208031
hg19208031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11723346
SamplesHG04029
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603344
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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