A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631630



Internal ID7018439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28089355..28090346hg38UCSC Ensembl
Innerchr13:28089489..28090279hg38UCSC Ensembl
Outerchr13:28089173..28090528hg38UCSC Ensembl
chr13:28663492..28664483hg19UCSC Ensembl
Innerchr13:28663626..28664416hg19UCSC Ensembl
Outerchr13:28663310..28664665hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38992
hg19992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14678428, essv14678418, essv14678423, essv14678422, essv14678421, essv14678426, essv14678430, essv14678425, essv14678427, essv14678424, essv14678420, essv14678429, essv14678419
SamplesHG03514, HG03096, HG03121, NA19355, HG03297, HG03105, HG02111, HG03301, NA19436, HG02010, NA19037, HG02971, HG02284
Known GenesFLT3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631630
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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