A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878455



Internal ID22653420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15729523..15752600hg38UCSC Ensembl
chr17:15632837..15655914hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3823078
hg1923078
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475489, nssv17475490
Samples
Known GenesTBC1D26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878455
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