A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471978



Internal ID22529870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:66998783..67040905hg38UCSC Ensembl
chr18:64666020..64708142hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3842123
hg1942123
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884108
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471978
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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