A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541019



Internal ID297619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6984112..6984162hg38UCSC Ensembl
chr6:6984345..6984395hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv419n206
Supporting Variantsnssv16978092
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541019
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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