A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686572



Internal ID110238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30107894..30108070hg38UCSC Ensembl
chr13:30682031..30682207hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500304
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686572
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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