A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603822



Internal ID6990853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1746881..1751613hg38UCSC Ensembl
Innerchr5:1746881..1751613hg38UCSC Ensembl
Outerchr5:1746628..1751866hg38UCSC Ensembl
chr5:1746996..1751728hg19UCSC Ensembl
Innerchr5:1746996..1751728hg19UCSC Ensembl
Outerchr5:1746743..1751981hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg384733
hg194733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11784552
SamplesHG03965
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603822
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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