A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610578



Internal ID21802625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111257423..111257423hg38UCSC Ensembl
chr12:111695227..111695227hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084761
Supporting Variants
Samples
Known GenesCUX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610578
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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