A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366382



Internal ID22592051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117394720..117395632hg38UCSC Ensembl
chr10:119154231..119155143hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915785
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366382
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