A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385381



Internal ID22443251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36456039..36456392hg38UCSC Ensembl
chr15:36748240..36748593hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947534
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385381
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