A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606561



Internal ID21798608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132733349..132733349hg38UCSC Ensembl
chr12:133309935..133309935hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092825
Supporting Variants
Samples
Known GenesANKLE2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606561
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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