A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17613823



Internal ID21805870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106100198..106100310hg38UCSC Ensembl
chr12:106493976..106494088hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025585
Supporting Variants
Samples
Known GenesNUAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17613823
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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