A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617561



Internal ID21809608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35926180..35926180hg38UCSC Ensembl
chr18:33506143..33506143hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110296
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617561
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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