A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595775



Internal ID21544382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37730189..37730626hg38UCSC Ensembl
chr19:38221090..38221527hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104793
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595775
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer