A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851515



Internal ID22626450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56007604..56027566hg38UCSC Ensembl
chr15:56299802..56319764hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3819963
hg1919963
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472912
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851515
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