A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647880



Internal ID21596185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36179244..36179244hg38UCSC Ensembl
chr19:36670146..36670146hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104506
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647880
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