A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842229



Internal ID22617164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178707688..178715484hg38UCSC Ensembl
chr5:178134689..178142485hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg387797
hg197797
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498414
Samples
Known GenesZNF354A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842229
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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