A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608701



Internal ID21800748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122226395..122226395hg38UCSC Ensembl
chr12:122710942..122710942hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097433
Supporting Variants
Samples
Known GenesDIABLO
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608701
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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