A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631631



Internal ID7018440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28090165..28091360hg38UCSC Ensembl
Innerchr13:28090215..28091310hg38UCSC Ensembl
Outerchr13:28090077..28091448hg38UCSC Ensembl
chr13:28664302..28665497hg19UCSC Ensembl
Innerchr13:28664352..28665447hg19UCSC Ensembl
Outerchr13:28664214..28665585hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg381196
hg191196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14678431
SamplesHG01130
Known GenesFLT3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631631
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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