A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288387



Internal ID20497605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55911173..55911173hg38UCSC Ensembl
chr14:56377891..56377891hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg381357
hg191357
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758329
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288387
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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