A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950226



Internal ID22725638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87001895..87001895hg38UCSC Ensembl
chr5:86297712..86297712hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414973
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950226
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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