A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466522



Internal ID22524414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28040394..28041643hg38UCSC Ensembl
chr13:28614531..28615780hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg381250
hg191250
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867395
Supporting Variants
Samples
Known GenesFLT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466522
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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