A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291780



Internal ID20500998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159270853..159270853hg38UCSC Ensembl
chr5:158697861..158697861hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766212
Supporting Variants
Samples
Known GenesUBLCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291780
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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