A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559991



Internal ID333009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77068981..77096473hg38UCSC Ensembl
chr17:75065063..75092555hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3827493
hg1927493
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725015
Samples
Known GenesLINC00338, MIR6516, SCARNA16, SEC14L1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559991
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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