A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272111



Internal ID20481329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90570668..90570668hg38UCSC Ensembl
chr13:91222922..91222922hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763924
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272111
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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