A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13706427



Internal ID21228225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34228124..34231420hg38UCSC Ensembl
chr20:32815930..32819226hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg383297
hg193297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2803101
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13706427
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency1


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