A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17393344



Internal ID22451214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78822325..78831168hg38UCSC Ensembl
chr18:76582325..76591168hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg388844
hg198844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937498
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17393344
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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