A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915684



Internal ID22690902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24952238..24963959hg38UCSC Ensembl
chr10:25241167..25252888hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3811722
hg1911722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361395
Samples
Known GenesPRTFDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915684
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