A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544402



Internal ID21868757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10458853..10458853hg38UCSC Ensembl
chr5:10458965..10458965hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6068120
Supporting Variants
Samples
Known GenesROPN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544402
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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