A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557825



Internal ID330911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96147326..96274352hg38UCSC Ensembl
chr5:95483030..95610056hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38127027
hg19127027
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557825
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