A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591056



Internal ID21539628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42436057..42436202hg38UCSC Ensembl
chr19:42940209..42940354hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105066
SamplesHG03486
Known GenesCXCL17, LIPE-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591056
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