A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510443



Internal ID287062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120714377..120715573hg38UCSC Ensembl
chr12:121152180..121153376hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17684928
Samples
Known GenesUNC119B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510443
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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