A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833105



Internal ID22608040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70813866..70829613hg38UCSC Ensembl
chr2:71040998..71056744hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3815748
hg1915747
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487997
Samples
Known GenesCLEC4F
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833105
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