A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479852



Internal ID22537754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78584546..78601997hg38UCSC Ensembl
chr18:76344546..76361997hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3817452
hg1917452
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878631
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479852
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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