A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485341



Internal ID22543252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35686809..35706611hg38UCSC Ensembl
chr20:34274731..34294533hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3819803
hg1919803
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874203
Supporting Variants
Samples
Known GenesNFS1, RBM39, ROMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485341
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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