A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369786



Internal ID22595455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28051794..28052343hg38UCSC Ensembl
chr13:28625931..28626480hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927635
Supporting Variants
Samples
Known GenesFLT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369786
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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