A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840482



Internal ID22615417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88382255..88387457hg38UCSC Ensembl
chr4:89303407..89308609hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg385203
hg195203
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497941
Samples
Known GenesHERC6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840482
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