A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857964



Internal ID22632899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104590206..104597749hg38UCSC Ensembl
chr14:105056543..105064086hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg387544
hg197544
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468521
Samples
Known GenesTMEM179
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857964
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