A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631627



Internal ID7018436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28042000..28044000hg38UCSC Ensembl
Innerchr13:28042000..28044000hg38UCSC Ensembl
Outerchr13:28041703..28044268hg38UCSC Ensembl
chr13:28616137..28618137hg19UCSC Ensembl
Innerchr13:28616137..28618137hg19UCSC Ensembl
Outerchr13:28615840..28618405hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg382001
hg192001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14678338, essv14678337
SamplesNA19466, HG01853
Known GenesFLT3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631627
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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