A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285419



Internal ID20494637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51400114..51400114hg38UCSC Ensembl
chr5:50695948..50695948hg19UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4768040
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285419
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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