A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615300



Internal ID21807347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55871380..55871380hg38UCSC Ensembl
chr12:56265164..56265164hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6093612
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615300
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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