A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624154



Internal ID21816201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6730219..6730219hg38UCSC Ensembl
chr18:6730218..6730218hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112481
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624154
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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