A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13688549



Internal ID21210405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11009488..11009488hg38UCSC Ensembl
chr20:10990136..10990136hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802371
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13688549
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.546875


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