A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537862



Internal ID313057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108719745..108719784hg38UCSC Ensembl
chr5:108055446..108055485hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537862
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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