A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5544845



Internal ID318948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53105838..53105889hg38UCSC Ensembl
chr12:53499622..53499673hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17058630
Samples
Known GenesSOAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5544845
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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