A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366144



Internal ID22591813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73109301..73109473hg38UCSC Ensembl
chr10:74869059..74869231hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914351
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366144
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