A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551211



Internal ID324689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118340877..118340911hg38UCSC Ensembl
chr6:118662040..118662074hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551211
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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