A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268089



Internal ID20477307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:52497378..52497378hg38UCSC Ensembl
chr18:50023748..50023748hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767825
Supporting Variants
Samples
Known GenesDCC
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268089
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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