A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603666



Internal ID21795713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93441528..93441528hg38UCSC Ensembl
chr12:93835304..93835304hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087718
Supporting Variants
Samples
Known GenesUBE2N
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603666
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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