A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104061



Internal ID21463745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2455154..2455154hg38UCSC Ensembl
chr19:2455152..2455152hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384997
hg194997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657344
Supporting Variants
SamplesHG03009
Known GenesLMNB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104061
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