A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17398576



Internal ID22456446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32494920..32494974hg38UCSC Ensembl
chr20:31082723..31082777hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5950752
Supporting Variants
Samples
Known GenesC20orf112
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17398576
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