A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931047



Internal ID22706324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41561637..41562544hg38UCSC Ensembl
chr15:41853835..41854742hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38908
hg19908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387001
Samples
Known GenesTYRO3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931047
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer