A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282958



Internal ID20492176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:130882155..130882558hg38UCSC Ensembl
chr12:131366700..131367103hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733218
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282958
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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