A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561925



Internal ID334891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151667491..151681542hg38UCSC Ensembl
chr1:151639967..151654018hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3814052
hg1914052
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890321
Samples
Known GenesSNX27
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561925
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