A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555824



Internal ID328973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149477283..149478496hg38UCSC Ensembl
chr5:148856846..148858059hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381214
hg191214
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974739
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555824
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