A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5407726



Internal ID187057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18167894..18167945hg38UCSC Ensembl
chr4:18169517..18169568hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5407726
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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