A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287617



Internal ID20496835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10414478..10414478hg38UCSC Ensembl
chr18:10414475..10414475hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765057
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287617
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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