A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021958



Internal ID21931301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:73206957..73263081hg38UCSC Ensembl
chr12:73600737..73656861hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3856125
hg1956125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021958
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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