A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270877



Internal ID20480095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169945793..169945793hg38UCSC Ensembl
chr4:170866944..170866944hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752375
Supporting Variants
Samples
Known GenesLOC100506085
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270877
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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