A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495346



Internal ID272464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50272262..50274303hg38UCSC Ensembl
chr12:50666045..50668086hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg382042
hg192042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17056474
Samples
Known GenesLIMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495346
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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