A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599670



Internal ID6986715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:12107872..12150175hg38UCSC Ensembl
Innerchr4:12107872..12150175hg38UCSC Ensembl
Outerchr4:12107372..12150675hg38UCSC Ensembl
chr4:12109496..12151799hg19UCSC Ensembl
Innerchr4:12109496..12151799hg19UCSC Ensembl
Outerchr4:12108996..12152299hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3842304
hg1942304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11357362
SamplesHG01781
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599670
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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