A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632673



Internal ID21824720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76975159..76975159hg38UCSC Ensembl
chr18:74687115..74687115hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105661
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632673
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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