A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14678427



Internal ID3867873
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3631630
Supporting Variants
SamplesHG03514
Known GenesFLT3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14678427
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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