A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478513



Internal ID22536414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:47641732..47651168hg38UCSC Ensembl
chr18:45168103..45177539hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg389437
hg199437
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873909
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478513
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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