A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419098



Internal ID22476968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168454758..168454758hg38UCSC Ensembl
chr4:169375909..169375909hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5949862
Supporting Variants
Samples
Known GenesDDX60L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419098
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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