A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867438



Internal ID22642373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72402885..72409285hg38UCSC Ensembl
chr15:72695226..72701626hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386401
hg196401
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473599
Samples
Known GenesTMEM202
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867438
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