A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556319



Internal ID21880674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126131540..126131540hg38UCSC Ensembl
chr5:125467233..125467233hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg386607
hg196607
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072017
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556319
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