A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485937



Internal ID22543850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3806383..3809394hg38UCSC Ensembl
chr20:3787030..3790041hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383012
hg193012
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880152
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485937
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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