A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391594



Internal ID22449464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:48917779..48918011hg38UCSC Ensembl
chr20:47534316..47534548hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5953225
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391594
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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