A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534509



Internal ID310300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:266873..266892hg38UCSC Ensembl
chr5:266988..267007hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534509
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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