A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271167



Internal ID20480385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21858055..21858055hg38UCSC Ensembl
chr14:22326232..22326232hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756273
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271167
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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