A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606294



Internal ID21798341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:114063802..114064631hg38UCSC Ensembl
chr12:114501607..114502436hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38830
hg19830
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025700
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606294
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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