A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456029



Internal ID22513906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68748616..68751424hg38UCSC Ensembl
chr14:69215333..69218141hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg382809
hg192809
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852117
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456029
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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