A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280105



Internal ID20489323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10681783..10681783hg38UCSC Ensembl
chr5:10681895..10681895hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761650
Supporting Variants
Samples
Known GenesDAP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280105
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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