A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413875



Internal ID22471745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69064448..69067860hg38UCSC Ensembl
chr5:68360275..68363687hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg383413
hg193413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895457
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413875
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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