A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096094



Internal ID21500586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85395634..85395634hg38UCSC Ensembl
chr13:85969769..85969769hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651316
Supporting Variants
SamplesNA19239
Known GenesLINC00351
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096094
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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