A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618367



Internal ID21810414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:51429089..51429089hg38UCSC Ensembl
chr18:48955459..48955459hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109344
Supporting Variants
Samples
Known GenesLOC100287225
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618367
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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