A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939610



Internal ID22715006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45594721..45594855hg38UCSC Ensembl
chr19:46097979..46098113hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406153
Samples
Known GenesGPR4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939610
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