A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14678431



Internal ID1283053
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3631631
Supporting Variants
SamplesHG01130
Known GenesFLT3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14678431
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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