A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859932



Internal ID22634867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32807795..32810544hg38UCSC Ensembl
chr12:32960729..32963478hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg382750
hg192750
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452728
Samples
Known GenesPKP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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