A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620135



Internal ID21812182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78769319..78769319hg38UCSC Ensembl
chr18:76529319..76529319hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104416
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620135
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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