A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694157



Internal ID117823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110385399..110386063hg38UCSC Ensembl
chr13:111037746..111038410hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494527
Supporting Variants
Samples
Known GenesCOL4A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694157
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.741724


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