A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100276



Internal ID22009509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12629962..12629962hg38UCSC Ensembl
chr12:12782896..12782896hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616918
Samples
Known GenesCREBL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100276
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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