A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353882



Internal ID22579551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21166095..21166095hg38UCSC Ensembl
chr1:21492588..21492588hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961218
Supporting Variants
Samples
Known GenesEIF4G3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353882
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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