A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021838



Internal ID21931181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27008636..27009461hg38UCSC Ensembl
chr12:27161569..27162394hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613632
Samples
Known GenesTM7SF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021838
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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