A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889455



Internal ID22664472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157799276..157801679hg38UCSC Ensembl
chr5:157226284..157228687hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg382404
hg192404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428773
Samples
Known GenesCLINT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889455
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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