A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898401



Internal ID22673515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153791156..153792353hg38UCSC Ensembl
chr5:153170716..153171913hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg381198
hg191198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427846
Samples
Known GenesGRIA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898401
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