A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852168



Internal ID22627103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96078894..96081025hg38UCSC Ensembl
chr12:96472672..96474803hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg382132
hg192132
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459961
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852168
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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