A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460408



Internal ID22518292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37889607..37896556hg38UCSC Ensembl
chr14:38358812..38365761hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg386950
hg196950
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460408
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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