A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17378143



Internal ID22436013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63405773..63407079hg38UCSC Ensembl
chr15:63697972..63699278hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381307
hg191307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929977
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17378143
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