A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617395



Internal ID21809442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119829242..119829242hg38UCSC Ensembl
chr12:120267046..120267046hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg383369
hg193369
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6096160
Supporting Variants
Samples
Known GenesCIT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617395
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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