A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478515



Internal ID22536416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48456597..48463634hg38UCSC Ensembl
chr18:45982968..45990005hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg387038
hg197038
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877083
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478515
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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