A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260217



Internal ID20469435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8212349..8212349hg38UCSC Ensembl
chr5:8212462..8212462hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765844
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260217
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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