A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479129



Internal ID22537031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55696419..55698318hg38UCSC Ensembl
chr18:53363650..53365549hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875327
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479129
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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