A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510374



Internal ID286995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132715272..132715580hg38UCSC Ensembl
chr12:133291858..133292166hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17685712
Samples
Known GenesPGAM5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510374
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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