A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621643



Internal ID21813690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:41348151..41348151hg38UCSC Ensembl
chr18:38928115..38928115hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112280
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621643
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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