A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091119



Internal ID22000352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:22869632..22869632hg38UCSC Ensembl
chr12:23022566..23022566hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600508
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091119
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer