A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552648



Internal ID21877003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169945779..169945779hg38UCSC Ensembl
chr4:170866930..170866930hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6066014
Supporting Variants
Samples
Known GenesLOC100506085
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552648
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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