A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285971



Internal ID20495189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58309483..58309483hg38UCSC Ensembl
chr20:56884539..56884539hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751088
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285971
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