A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420679



Internal ID22478549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97049171..97049171hg38UCSC Ensembl
chr4:97970322..97970322hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959911
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420679
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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