A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088599



Internal ID21482294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56860998..56860998hg38UCSC Ensembl
chr15:57153196..57153196hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644849
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088599
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