A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551852



Internal ID325274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6984112..6984153hg38UCSC Ensembl
chr6:6984345..6984386hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv419n206
Supporting Variantsnssv16978093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551852
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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