A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295134



Internal ID20504352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53072029..53072029hg38UCSC Ensembl
chr13:53646164..53646164hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752208
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295134
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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