A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17578375



Internal ID21770418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4853114..4853114hg38UCSC Ensembl
chr9:4853114..4853114hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg385946
hg195946
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085050
Supporting Variants
Samples
Known GenesRCL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17578375
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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