A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895852



Internal ID22670939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157680628..157719093hg38UCSC Ensembl
chr5:157107636..157146101hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3838466
hg1938466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895852
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer