A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377006



Internal ID22434876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99377287..99418130hg38UCSC Ensembl
chr15:99917492..99958335hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3840844
hg1940844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933622
Supporting Variants
Samples
Known GenesLRRC28
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377006
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