A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17057386



Internal ID106102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25452025..25459740hg38UCSC Ensembl
chr12:25604959..25612674hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg387716
hg197716
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559657
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17057386
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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