A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902422



Internal ID22677581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73384899..73445669hg38UCSC Ensembl
chr5:72680726..72741496hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3860771
hg1960771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414613
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902422
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