A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17379608



Internal ID22437478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79607611..79607611hg38UCSC Ensembl
chr13:80181746..80181746hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980262
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17379608
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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