A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14678341



Internal ID2660000
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3631628
Supporting Variants
SamplesHG02353
Known GenesFLT3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14678341
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer