A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563174



Internal ID21887529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160445520..160445520hg38UCSC Ensembl
chr5:159872527..159872527hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072384
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563174
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