A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987791



Internal ID59301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104417803..104503929hg38UCSC Ensembl
chr6:104865678..104951804hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3886127
hg1986127
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555079
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987791
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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