A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286873



Internal ID20496091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27214121..27214121hg38UCSC Ensembl
chr13:27788258..27788258hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760619
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286873
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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