A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646624



Internal ID21594929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2445552..2445552hg38UCSC Ensembl
chr19:2445550..2445550hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104060
SamplesHG02818
Known GenesLMNB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646624
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