A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185005



Internal ID20752045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28043849..28044392hg38UCSC Ensembl
chr13:28617986..28618529hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476163
Supporting Variants
Samples
Known GenesFLT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185005
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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