A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915432



Internal ID22690650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84287310..84287365hg38UCSC Ensembl
chr8:85199545..85199600hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437685
Samples
Known GenesRALYL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915432
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