A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426433



Internal ID22484303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:50345031..51260939hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38915909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895736
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426433
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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