A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022403



Internal ID21931746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101625645..101625756hg38UCSC Ensembl
chr12:102019423..102019534hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604331
Samples
Known GenesMYBPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022403
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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