A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276139



Internal ID20485357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55971192..55971192hg38UCSC Ensembl
chr14:56437910..56437910hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756778
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276139
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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