A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094151



Internal ID22003384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10334173..10334173hg38UCSC Ensembl
chr12:10486772..10486772hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094151
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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