A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614981



Internal ID21807028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64589323..64589323hg38UCSC Ensembl
chr12:64983103..64983103hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6098843
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614981
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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