A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010789



Internal ID21920132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2176588..2177588hg38UCSC Ensembl
chr9:2176588..2177588hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582463
Samples
Known GenesSMARCA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010789
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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