A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537076



Internal ID312431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194209339..194209364hg38UCSC Ensembl
chr3:193927128..193927153hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944485
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537076
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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