A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497662



Internal ID274688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120478263..120478371hg38UCSC Ensembl
chr12:120916066..120916174hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17684909
Samples
Known GenesDYNLL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497662
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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