A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295254



Internal ID20504472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79921784..79921784hg38UCSC Ensembl
chr14:80388127..80388127hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755641
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295254
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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