A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456900



Internal ID22514780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76535488..76543611hg38UCSC Ensembl
chr14:77001831..77009954hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg388124
hg198124
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858195
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456900
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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