A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17424426



Internal ID22482296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164353303..164420716hg38UCSC Ensembl
chr5:163780309..163847722hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3867414
hg1967414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17424426
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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