A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602372



Internal ID6989406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:136618649..136703597hg38UCSC Ensembl
Innerchr4:136619149..136703097hg38UCSC Ensembl
Outerchr4:136617649..136704597hg38UCSC Ensembl
chr4:137539804..137624752hg19UCSC Ensembl
Innerchr4:137540304..137624252hg19UCSC Ensembl
Outerchr4:137538804..137625752hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3884949
hg1984949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11621063, essv11621062, essv11621061, essv11621060
SamplesHG02356, HG02047, HG02367, HG01805
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602372
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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