A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052863



Internal ID103091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9998359..10039183hg38UCSC Ensembl
chr12:10150958..10191782hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3840825
hg1940825
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559751
Supporting Variants
Samples
Known GenesCLEC12B, CLEC1B, CLEC9A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052863
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.242273


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