A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958217



Internal ID22733293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168491947..168491947hg38UCSC Ensembl
chr4:169413098..169413098hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958217
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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