A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355825



Internal ID22581494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2580097..2636530hg38UCSC Ensembl
chr10:2622289..2678722hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3856434
hg1956434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355825
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