A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538608



Internal ID21862963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122799110..122799110hg38UCSC Ensembl
chr5:122134805..122134805hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg382584
hg192584
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6068418
Supporting Variants
Samples
Known GenesSNX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538608
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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