A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897603



Internal ID22672707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87660835..87661961hg38UCSC Ensembl
chr5:86956652..86957778hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381127
hg191127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413298
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897603
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