A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560538



Internal ID333544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9403162..9570529hg38UCSC Ensembl
chr12:9555758..9723125hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38167368
hg19167368
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17055833
Samples
Known GenesDDX12P
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560538
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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