A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602396



Internal ID6989430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137465390..137479154hg38UCSC Ensembl
Innerchr4:137465390..137479154hg38UCSC Ensembl
Outerchr4:137464890..137479654hg38UCSC Ensembl
chr4:138386544..138400308hg19UCSC Ensembl
Innerchr4:138386544..138400308hg19UCSC Ensembl
Outerchr4:138386044..138400808hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3813765
hg1913765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11629792
SamplesHG01603
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602396
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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