A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891065



Internal ID22666098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69371169..69373826hg38UCSC Ensembl
chr5:68666996..68669653hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg382658
hg192658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426996
Samples
Known GenesRAD17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891065
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