A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556840



Internal ID329965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155325949..155326000hg38UCSC Ensembl
chr6:155647083..155647134hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385998
hg195998
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556840
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer