A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599986



Internal ID21792033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109349412..109359175hg38UCSC Ensembl
chr12:109787217..109796980hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg389764
hg199764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022638
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599986
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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