A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552243



Internal ID21876598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186299782..186299782hg38UCSC Ensembl
chr4:187220936..187220936hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074050
Supporting Variants
Samples
Known GenesF11-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552243
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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