A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2802928



Internal ID21248266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38122394..38122455hg38UCSC Ensembl
chr20:36750796..36750857hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687733
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2802928
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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