A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619747



Internal ID21811794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4686661..4700805hg38UCSC Ensembl
chr18:4686661..4700805hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3814145
hg1914145
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039239
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619747
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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