A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839222



Internal ID22614157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20405925..20406924hg38UCSC Ensembl
chr4:20407548..20408547hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492797
Samples
Known GenesSLIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839222
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