A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929286



Internal ID22704537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47629036..47629691hg38UCSC Ensembl
chr19:48132293..48132948hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398800
Samples
Known GenesGLTSCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929286
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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