A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611771



Internal ID21803818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43076823..43076823hg38UCSC Ensembl
chr15:43369021..43369021hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092434
Supporting Variants
Samples
Known GenesUBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611771
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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