A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106385



Internal ID21494122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56909107..56909107hg38UCSC Ensembl
chr19:57420475..57420475hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652099
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106385
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