A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849446



Internal ID22624381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74045864..74046963hg38UCSC Ensembl
chr14:74512567..74513666hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455127
Samples
Known GenesCCDC176
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849446
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