A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17554523



Internal ID21878878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26297110..26297110hg38UCSC Ensembl
chr5:26297219..26297219hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063196
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17554523
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