A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098659



Internal ID21500158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:69884926..69885239hg38UCSC Ensembl
chr13:70459058..70459371hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588506
Supporting Variants
SamplesNA19239
Known GenesKLHL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098659
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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