A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380511



Internal ID22438381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:49734122..49739871hg38UCSC Ensembl
chr18:47260492..47266241hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg385750
hg195750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945872
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380511
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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