A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845438



Internal ID22620373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7378554..7427787hg38UCSC Ensembl
chr6:7378787..7428020hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3849234
hg1949234
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507978
Samples
Known GenesCAGE1, RIOK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845438
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