A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289642



Internal ID20498860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:125204207..125204676hg38UCSC Ensembl
chr12:125688753..125689222hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747448
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289642
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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