A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286597



Internal ID20495815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113665078..113665142hg38UCSC Ensembl
chr12:114102883..114102947hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749412
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286597
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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