A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411646



Internal ID22469516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:92341160..92348738hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg387579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411646
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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