A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370013



Internal ID22595682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:59525231..59525231hg38UCSC Ensembl
chr13:60099365..60099365hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970412
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370013
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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