A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631628



Internal ID7018437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28080366..28100330hg38UCSC Ensembl
Innerchr13:28080866..28099830hg38UCSC Ensembl
Outerchr13:28079366..28101330hg38UCSC Ensembl
chr13:28654503..28674467hg19UCSC Ensembl
Innerchr13:28655003..28673967hg19UCSC Ensembl
Outerchr13:28653503..28675467hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3819965
hg1919965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14678340, essv14678339, essv14678341
SamplesHG02070, HG02186, HG02353
Known GenesFLT3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631628
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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