A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098651



Internal ID22007884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:28916428..28916428hg38UCSC Ensembl
chr12:29069361..29069361hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098651
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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