A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024487



Internal ID21933830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103222892..103222993hg38UCSC Ensembl
chr12:103616670..103616771hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024487
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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