A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292253



Internal ID20501471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76276332..76276384hg38UCSC Ensembl
chr12:76670112..76670164hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738517
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292253
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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