A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093179



Internal ID22002412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5617184..5617184hg38UCSC Ensembl
chr12:5726350..5726350hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614760
Samples
Known GenesANO2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093179
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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