A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479632



Internal ID22537534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38835466..38846093hg38UCSC Ensembl
chr18:36415430..36426057hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3810628
hg1910628
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479632
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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