A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15193468



Internal ID21332364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28065648..28065648hg38UCSC Ensembl
chr13:28639785..28639785hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945474
Supporting Variants
SamplesHG002
Known GenesFLT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15193468
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer