A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352865



Internal ID22578534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128209288..128209338hg38UCSC Ensembl
chr10:130007552..130007602hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5913841
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352865
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