A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485377



Internal ID22543288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37043157..37044575hg38UCSC Ensembl
chr20:35671560..35672978hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381419
hg191419
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876707
Supporting Variants
Samples
Known GenesRBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485377
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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