A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735287



Internal ID20511229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25349355..25349903hg38UCSC Ensembl
chr10:25638284..25638832hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281831
Samples
Known GenesGPR158
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735287
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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