A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599093



Internal ID6986141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:191192059..191204244hg38UCSC Ensembl
Innerchr3:191192559..191203744hg38UCSC Ensembl
Outerchr3:191191059..191205244hg38UCSC Ensembl
chr3:190909848..190922033hg19UCSC Ensembl
Innerchr3:190910348..190921533hg19UCSC Ensembl
Outerchr3:190908848..190923033hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3812186
hg1912186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11269506, essv11269507, essv11269508
SamplesHG03926, HG03642, HG01920
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599093
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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