A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594180



Internal ID21786223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40116387..40116387hg38UCSC Ensembl
chr8:39973906..39973906hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg381727
hg191727
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072206
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594180
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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